NO751314L - - Google Patents

Info

Publication number: NO751314L
Authority: NO; Norway
Prior art keywords: bis; pyridine; reaction; trichloro; mixture
Prior art date: 1974-04-15

Application number

NO751314A

Other languages

English (en)

Norwegian (no)

Inventor

P A Domenico

Original Assignee

Dow Chemical Co

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.)

1974-04-15

Filing date

1975-04-14

Publication date

1975-10-16

1975-04-14 Application filed by Dow Chemical Co filed Critical Dow Chemical Co

1975-10-16 Publication of NO751314L publication Critical patent/NO751314L/no

Links

239000000460 chlorine Substances 0.000 claims description 3
229910052801 chlorine Inorganic materials 0.000 claims description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Chemical group 0.000 claims description 2
DOJKHTWRFHKSFU-UHFFFAOYSA-N [2,3,5-trichloro-6-(thiocyanatomethylsulfanyl)-1H-pyridin-2-yl]sulfanylmethyl thiocyanate Chemical group ClC1=C(NC(C(=C1)Cl)(SCSC#N)Cl)SCSC#N DOJKHTWRFHKSFU-UHFFFAOYSA-N 0.000 claims 1
125000001309 chloro group Chemical group Cl* 0.000 claims 1
230000000361 pesticidal effect Effects 0.000 claims 1
JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 15
150000001875 compounds Chemical class 0.000 description 9
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 7
239000000203 mixture Substances 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
239000003440 toxic substance Substances 0.000 description 5
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
239000000463 material Substances 0.000 description 4
231100000167 toxic agent Toxicity 0.000 description 4
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 3
239000003973 paint Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
239000004753 textile Substances 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 2
239000010730 cutting oil Substances 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000003292 glue Substances 0.000 description 2
239000000976 ink Substances 0.000 description 2
239000003921 oil Substances 0.000 description 2
239000000376 reactant Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
239000000344 soap Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
CXURGFRDGROIKG-UHFFFAOYSA-N 3,3-bis(chloromethyl)oxetane Chemical compound ClCC1(CCl)COC1 CXURGFRDGROIKG-UHFFFAOYSA-N 0.000 description 1
XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
241001465318 Aspergillus terreus Species 0.000 description 1
244000063299 Bacillus subtilis Species 0.000 description 1
235000014469 Bacillus subtilis Nutrition 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
241000208680 Hamamelis mollis Species 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
241000187481 Mycobacterium phlei Species 0.000 description 1
SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
241001045770 Trichophyton mentagrophytes Species 0.000 description 1
239000008272 agar Substances 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
230000001580 bacterial effect Effects 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
210000000988 bone and bone Anatomy 0.000 description 1
-1 building boards Substances 0.000 description 1
229910052792 caesium Inorganic materials 0.000 description 1
TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
244000053095 fungal pathogen Species 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000001963 growth medium Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
239000005457 ice water Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
238000000034 method Methods 0.000 description 1
244000005700 microbiome Species 0.000 description 1
LCEDQNDDFOCWGG-UHFFFAOYSA-N morpholine-4-carbaldehyde Chemical compound O=CN1CCOCC1 LCEDQNDDFOCWGG-UHFFFAOYSA-N 0.000 description 1
239000004570 mortar (masonry) Substances 0.000 description 1
229940055036 mycobacterium phlei Drugs 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000006916 nutrient agar Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000011505 plaster Substances 0.000 description 1
231100000614 poison Toxicity 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 1
229940116357 potassium thiocyanate Drugs 0.000 description 1
239000000843 powder Substances 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
229910052701 rubidium Inorganic materials 0.000 description 1
IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000012265 solid product Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000000271 synthetic detergent Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
229940118846 witch hazel Drugs 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/70—Sulfur atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Pyridine Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Fats And Perfumes (AREA)
Compositions Of Macromolecular Compounds (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

NO751314A 1974-04-15 1975-04-14 NO751314L (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US461063A US3894035A (en)	1974-04-15	1974-04-15	Bis-(thioalkylthio cyanato)halo pyridines

Publications (1)

Publication Number	Publication Date
NO751314L true NO751314L (de)	1975-10-16

Family

ID=23831074

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO751314A NO751314L (de)	1974-04-15	1975-04-14

Country Status (8)

Country	Link
US (1)	US3894035A (de)
JP (1)	JPS50140461A (de)
CA (1)	CA1027569A (de)
DE (1)	DE2515773A1 (de)
ES (1)	ES436374A1 (de)
GB (1)	GB1472022A (de)
NL (1)	NL7504115A (de)
NO (1)	NO751314L (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4994252A (en) *	1990-02-09	1991-02-19	Dowelanco	Removal of potassium chloride from solvents
JP2587377Y2 (ja) *	1992-02-17	1998-12-16	日本バイリーン株式会社	作業用ワイパー
WO1998054139A1 (de) *	1997-05-30	1998-12-03	Basf Aktiengesellschaft	Verfahren zur herstellung substituierter thiopyridine

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3758482A (en) *	1971-06-30	1973-09-11	Dow Chemical Co	Halopyridyl thiocyanates
US3787425A (en) *	1973-02-09	1974-01-22	Dow Chemical Co	Halopyridyl thiocyanates
US3787422A (en) *	1973-02-09	1974-01-22	Dow Chemical Co	Halopyridyl thiocyanates

1974
- 1974-04-15 US US461063A patent/US3894035A/en not_active Expired - Lifetime
1975
- 1975-04-07 ES ES436374A patent/ES436374A1/es not_active Expired
- 1975-04-07 NL NL7504115A patent/NL7504115A/xx unknown
- 1975-04-08 CA CA224,021A patent/CA1027569A/en not_active Expired
- 1975-04-09 GB GB1460075A patent/GB1472022A/en not_active Expired
- 1975-04-10 JP JP50043861A patent/JPS50140461A/ja active Pending
- 1975-04-10 DE DE19752515773 patent/DE2515773A1/de active Pending
- 1975-04-14 NO NO751314A patent/NO751314L/no unknown

Also Published As

Publication number	Publication date
US3894035A (en)	1975-07-08
NL7504115A (nl)	1975-10-17
ES436374A1 (es)	1977-01-16
DE2515773A1 (de)	1975-10-23
CA1027569A (en)	1978-03-07
JPS50140461A (de)	1975-11-11
GB1472022A (en)	1977-04-27

Publication	Publication Date	Title
CA1180708A (en)	1985-01-08	Process for preparing organic sulphides
NO751314L (de)	1975-10-16
US3641004A (en)	1972-02-08	Alkyl esters of 6-(benzenesulfonyl)-trihalo-2-picolinic acid
US3758482A (en)	1973-09-11	Halopyridyl thiocyanates
US3113144A (en)	1963-12-03	Organo-tin oxides
US3027371A (en)	1962-03-27	Molybdenum-containing derivatives of 1-hydroxy-2-pyridinethiones and method of preparing same
US3787422A (en)	1974-01-22	Halopyridyl thiocyanates
US3639413A (en)	1972-02-01	(thio- sulfinyl- and sulfonyl) containing pyridine compounds
US3787425A (en)	1974-01-22	Halopyridyl thiocyanates
US3850929A (en)	1974-11-26	(1,2,5)thiadiazolo(3,4-b)pyrazines
US3393209A (en)	1968-07-16	Furfuryl and tetrahydrofurfuryl phenyl ureas
US2922792A (en)	1960-01-26	Certain ester derivatives of 2-mercaptopyridine, n-oxide
CN109206363A (zh)	2019-01-15	一种制备2-氯烟酸的绿色新工艺
US3591596A (en)	1971-07-06	1,2-dihydro - 6 -methyl-2-oxo-4-pyridyl esters of certain benzene sulfonic acids and derivatives thereof
US2394902A (en)	1946-02-12	Preparation of substituted sulphonamides
NO751311L (de)	1975-10-16
US3117146A (en)	1964-01-07	Organotin hydroxides
NO751313L (de)	1975-10-16
EP0018100B1 (de)	1984-01-18	Substituierte, aromatische, biologisch wirksame Verbindung, Verfahren zu ihrer Herstellung und ihre Verwendung als Biozid
US3895016A (en)	1975-07-15	Halopyridyl thioalkylthio cyanates
US3674795A (en)	1972-07-04	Pyridyl xanthates
US3635994A (en)	1972-01-18	Halopyridine sulfenyl- and sulfonylhalides
US3711271A (en)	1973-01-16	Method for controlling algae
US3226427A (en)	1965-12-28	Carbamate thiosulfonates
US3725421A (en)	1973-04-03	(thio-, sulfinyl-{11 and sulfonyl) containing pyridine compounds