SE446730B - Forfarande for framstellning av trisubstituerade s-triazinforeningar - Google Patents

Forfarande for framstellning av trisubstituerade s-triazinforeningar

Info

Publication number: SE446730B
Authority: SE; Sweden
Prior art keywords: cyanuric chloride; general formula; container; compounds; atom
Prior art date: 1978-11-20

Application number

SE7909569A

Other languages

English (en)

Swedish (sv)

Other versions

SE7909569L (sv

Inventor

K Hentschel

F Bittner

Original Assignee

Degussa

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1978-11-20

Filing date

1979-11-19

Publication date

1986-10-06

1979-11-19 Application filed by Degussa filed Critical Degussa

1980-05-21 Publication of SE7909569L publication Critical patent/SE7909569L/xx

1986-10-06 Publication of SE446730B publication Critical patent/SE446730B/sv

Links

238000000034 method Methods 0.000 title claims description 14
JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical class C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 title claims description 4
MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 claims description 33
239000007788 liquid Substances 0.000 claims description 31
238000002156 mixing Methods 0.000 claims description 19
125000004432 carbon atom Chemical group C* 0.000 claims description 18
125000000217 alkyl group Chemical group 0.000 claims description 14
150000001875 compounds Chemical class 0.000 claims description 11
125000003342 alkenyl group Chemical group 0.000 claims description 10
239000003513 alkali Substances 0.000 claims description 9
150000001412 amines Chemical class 0.000 claims description 9
239000007921 spray Substances 0.000 claims description 9
238000006243 chemical reaction Methods 0.000 claims description 8
125000000753 cycloalkyl group Chemical group 0.000 claims description 6
-1 pyrrolidino, morpholino Chemical group 0.000 claims description 5
239000011541 reaction mixture Substances 0.000 claims description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
150000001298 alcohols Chemical class 0.000 claims description 4
125000003710 aryl alkyl group Chemical group 0.000 claims description 4
239000000460 chlorine Substances 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
238000005507 spraying Methods 0.000 claims description 4
NJYFRQQXXXRJHK-UHFFFAOYSA-N (4-aminophenyl) thiocyanate Chemical class NC1=CC=C(SC#N)C=C1 NJYFRQQXXXRJHK-UHFFFAOYSA-N 0.000 claims description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
125000004414 alkyl thio group Chemical group 0.000 claims description 3
125000004429 atom Chemical group 0.000 claims description 3
UAZDIGCOBKKMPU-UHFFFAOYSA-O azanium;azide Chemical class [NH4+].[N-]=[N+]=[N-] UAZDIGCOBKKMPU-UHFFFAOYSA-O 0.000 claims description 3
125000005843 halogen group Chemical group 0.000 claims description 3
238000010438 heat treatment Methods 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
229910052745 lead Inorganic materials 0.000 claims description 3
WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical group [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 claims description 3
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 3
229910052753 mercury Inorganic materials 0.000 claims description 3
125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
229910052709 silver Inorganic materials 0.000 claims description 3
150000003378 silver Chemical group 0.000 claims description 3
125000004434 sulfur atom Chemical group 0.000 claims description 3
229910052725 zinc Inorganic materials 0.000 claims description 3
239000011701 zinc Substances 0.000 claims description 3
KYLIZBIRMBGUOP-UHFFFAOYSA-N Anetholtrithion Chemical group C1=CC(OC)=CC=C1C1=CC(=S)SS1 KYLIZBIRMBGUOP-UHFFFAOYSA-N 0.000 claims description 2
101100037762 Caenorhabditis elegans rnh-2 gene Proteins 0.000 claims description 2
241000546339 Trioxys Species 0.000 claims description 2
239000011261 inert gas Substances 0.000 claims description 2
238000002844 melting Methods 0.000 claims description 2
230000008018 melting Effects 0.000 claims description 2
238000002360 preparation method Methods 0.000 claims description 2
238000004544 sputter deposition Methods 0.000 claims description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
230000007306 turnover Effects 0.000 claims 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
239000002904 solvent Substances 0.000 description 7
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
239000000463 material Substances 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 5
125000001424 substituent group Chemical group 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
239000000203 mixture Substances 0.000 description 4
239000000243 solution Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000009826 distribution Methods 0.000 description 3
238000005516 engineering process Methods 0.000 description 3
239000000155 melt Substances 0.000 description 3
239000002245 particle Substances 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
239000000370 acceptor Substances 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
125000004430 oxygen atom Chemical group O* 0.000 description 2
125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
NESLWCLHZZISNB-UHFFFAOYSA-M sodium phenolate Chemical compound [Na+].[O-]C1=CC=CC=C1 NESLWCLHZZISNB-UHFFFAOYSA-M 0.000 description 2
238000006467 substitution reaction Methods 0.000 description 2
239000000725 suspension Substances 0.000 description 2
IYDYVVVAQKFGBS-UHFFFAOYSA-N 2,4,6-triphenoxy-1,3,5-triazine Chemical compound N=1C(OC=2C=CC=CC=2)=NC(OC=2C=CC=CC=2)=NC=1OC1=CC=CC=C1 IYDYVVVAQKFGBS-UHFFFAOYSA-N 0.000 description 1
BIEFDNUEROKZRA-UHFFFAOYSA-N 2-(2-phenylethenyl)aniline Chemical compound NC1=CC=CC=C1C=CC1=CC=CC=C1 BIEFDNUEROKZRA-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
229910001854 alkali hydroxide Inorganic materials 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
HOPRXXXSABQWAV-UHFFFAOYSA-N anhydrous collidine Natural products CC1=CC=NC(C)=C1C HOPRXXXSABQWAV-UHFFFAOYSA-N 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
SJXIVKQAVJISKW-UHFFFAOYSA-N chloro cyanate Chemical compound ClOC#N SJXIVKQAVJISKW-UHFFFAOYSA-N 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
UTBIMNXEDGNJFE-UHFFFAOYSA-N collidine Natural products CC1=CC=C(C)C(C)=N1 UTBIMNXEDGNJFE-UHFFFAOYSA-N 0.000 description 1
239000004035 construction material Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
235000020095 red wine Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 description 1
UNHKSXOTUHOTAB-UHFFFAOYSA-N sodium;sulfane Chemical compound [Na].S UNHKSXOTUHOTAB-UHFFFAOYSA-N 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
GFYHSKONPJXCDE-UHFFFAOYSA-N sym-collidine Natural products CC1=CN=C(C)C(C)=C1 GFYHSKONPJXCDE-UHFFFAOYSA-N 0.000 description 1
230000007704 transition Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J10/00—Chemical processes in general for reacting liquid with gaseous media other than in the presence of solid particles, or apparatus specially adapted therefor
- B01J10/02—Chemical processes in general for reacting liquid with gaseous media other than in the presence of solid particles, or apparatus specially adapted therefor of the thin-film type
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/26—Nozzle-type reactors, i.e. the distribution of the initial reactants within the reactor is effected by their introduction or injection through nozzles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/30—Only oxygen atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Physical Or Chemical Processes And Apparatus (AREA)
Treating Waste Gases (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

SE7909569A 1978-11-20 1979-11-19 Forfarande for framstellning av trisubstituerade s-triazinforeningar SE446730B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2850338A DE2850338B2 (de)	1978-11-20	1978-11-20	Verfahren zur Herstellung von trisubstituierten s-Trianzinverbindungen

Publications (2)

Publication Number	Publication Date
SE7909569L SE7909569L (sv)	1980-05-21
SE446730B true SE446730B (sv)	1986-10-06

Family

ID=6055172

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE7909569A SE446730B (sv)	1978-11-20	1979-11-19	Forfarande for framstellning av trisubstituerade s-triazinforeningar

Country Status (19)

Country	Link
US (1)	US4281123A (de)
JP (1)	JPS5573668A (de)
AT (1)	AT368143B (de)
BE (1)	BE880141A (de)
BR (1)	BR7907283A (de)
CA (1)	CA1131634A (de)
CH (1)	CH644600A5 (de)
DD (1)	DD147105A5 (de)
DE (1)	DE2850338B2 (de)
ES (1)	ES483875A1 (de)
FR (1)	FR2441618A1 (de)
GB (1)	GB2036735B (de)
IL (1)	IL58607A (de)
IN (1)	IN153838B (de)
IT (1)	IT1119140B (de)
NL (1)	NL7908437A (de)
SE (1)	SE446730B (de)
YU (1)	YU40229B (de)
ZA (1)	ZA796281B (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS58210072A (ja) *	1982-05-18	1983-12-07	チバ―ガイギ　アクチエンゲゼルシヤフト	塩化シアヌ−ルの水中懸濁物の製造または塩化シアヌ−ルとアンモニアまたはアミンとの反応のための方法および装置
US4552959A (en) *	1982-05-18	1985-11-12	Ciba Geigy Ag	Process for producing a suspension of cyanuric chloride in water
DE4016159A1 (de) *	1990-05-19	1991-11-21	Bayer Ag	Verfahren zur kontinuierlichen umsetzung von cyanurfluorid mit aminen sowie reaktor zur durchfuehrung des verfahrens
US5290460A (en) *	1993-02-22	1994-03-01	Exxon Research & Engineering Co.	Lubricant composition containing complexes of alkoxylated amine, trithiocyanuric acid, and adenine
US5275745A (en) *	1993-02-22	1994-01-04	Exxon Research & Engineering Co.	Lubricant composition containing alkoxylated amine salt of trithiocyanuric acid
US5420274A (en) *	1993-10-19	1995-05-30	Ciba-Geigy Corporation	Process for the preparation of 2,4-di(alkylamino)-6-alkylthio-s-triazines

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1670585U (de)	1953-11-13	1954-01-21	Erich Breyer	Einrichtung zum anfeuchten und feuchthalten von wickeln, umschlaegen od. dgl.
FR1239784A (fr)	1958-11-05	1960-12-09	Geigy Ag J R	Nouveaux composés triaziniques à propriétés herbicides et leur préparation
NL131196C (de)	1966-07-16
DD111378A5 (de) *	1973-06-27	1975-02-12

1978
- 1978-11-20 DE DE2850338A patent/DE2850338B2/de not_active Withdrawn
1979
- 1979-07-16 YU YU1721/79A patent/YU40229B/xx unknown
- 1979-08-09 IT IT68647/79A patent/IT1119140B/it active
- 1979-08-29 IN IN900/CAL/79A patent/IN153838B/en unknown
- 1979-09-04 ES ES483875A patent/ES483875A1/es not_active Expired
- 1979-10-25 DD DD79216465A patent/DD147105A5/de unknown
- 1979-11-01 IL IL58607A patent/IL58607A/xx unknown
- 1979-11-09 BR BR7907283A patent/BR7907283A/pt unknown
- 1979-11-13 GB GB7939169A patent/GB2036735B/en not_active Expired
- 1979-11-16 US US06/094,873 patent/US4281123A/en not_active Expired - Lifetime
- 1979-11-19 AT AT0735279A patent/AT368143B/de not_active IP Right Cessation
- 1979-11-19 SE SE7909569A patent/SE446730B/sv not_active Application Discontinuation
- 1979-11-19 NL NL7908437A patent/NL7908437A/nl not_active Application Discontinuation
- 1979-11-19 CA CA340,144A patent/CA1131634A/en not_active Expired
- 1979-11-19 BE BE6/47015A patent/BE880141A/fr not_active IP Right Cessation
- 1979-11-19 CH CH1030479A patent/CH644600A5/de not_active IP Right Cessation
- 1979-11-20 JP JP14963179A patent/JPS5573668A/ja active Pending
- 1979-11-20 FR FR7928609A patent/FR2441618A1/fr active Granted
- 1979-11-20 ZA ZA00796281A patent/ZA796281B/xx unknown

Also Published As

Publication number	Publication date
GB2036735A (en)	1980-07-02
AT368143B (de)	1982-09-10
YU172179A (en)	1983-01-21
DE2850338B2 (de)	1981-05-07
IL58607A0 (en)	1980-02-29
ES483875A1 (es)	1980-05-16
DE2850338A1 (de)	1980-05-22
JPS5573668A (en)	1980-06-03
IT1119140B (it)	1986-03-03
DD147105A5 (de)	1981-03-18
ATA735279A (de)	1982-01-15
CA1131634A (en)	1982-09-14
ZA796281B (en)	1980-11-26
GB2036735B (en)	1983-03-09
NL7908437A (nl)	1980-05-22
US4281123A (en)	1981-07-28
BE880141A (fr)	1980-05-19
BR7907283A (pt)	1980-09-23
YU40229B (en)	1985-08-31
IL58607A (en)	1984-03-30
CH644600A5 (de)	1984-08-15
IN153838B (de)	1984-08-18
SE7909569L (sv)	1980-05-21
FR2441618A1 (fr)	1980-06-13
IT7968647A0 (it)	1979-08-09
FR2441618B1 (de)	1983-08-05

Legal Events

Date

Code

Title

Description

1995-02-28

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US2524081A (en)	1950-10-03	Preparation of thiuram monosulfides
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Morgan et al.	1920	LXXXIV.—Diphenylarsenious chloride and cyanide.(Diphenylchloroarsine and diphenylcyanoarsine.)
SE446728B (sv)	1986-10-06	Forfarande for framstellning av suspensioner eller losningar av cyanurklorid i vattenhaltiga organiska losningsmedel
NL7908433A (nl)	1980-05-22	Werkwijze voor het bereiden van suspensies of oplossingen van cyanuurchloride in organische oplosmiddelen.
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SE125815C1 (de)	1949-01-01
CH621541A5 (en)	1981-02-13	Process for the transesterification of esters of thiocarbamic acids