NO751316L - - Google Patents

Info

Publication number: NO751316L
Authority: NO; Norway
Prior art keywords: weight; compound; trichloro; benzene; thiocyanatomethylthio
Prior art date: 1974-04-15

Application number

NO751316A

Other languages

English (en)

Norwegian (no)

Inventor

C T Goralski

R G Pews

G A Burk

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 NO751316L publication Critical patent/NO751316L/no

Links

150000001875 compounds Chemical class 0.000 claims description 37
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 24
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
239000000460 chlorine Substances 0.000 claims description 8
229910052801 chlorine Inorganic materials 0.000 claims description 8
-1 2,3,6-trichloro-1-(thiocyanatomethylthio)benzene Chemical group 0.000 claims description 7
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
229910052794 bromium Inorganic materials 0.000 claims description 3
125000001246 bromo group Chemical group Br* 0.000 claims description 2
150000001555 benzenes Chemical class 0.000 claims 1
229920001817 Agar Polymers 0.000 description 12
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
239000008272 agar Substances 0.000 description 12
238000002474 experimental method Methods 0.000 description 11
239000003440 toxic substance Substances 0.000 description 9
231100000167 toxic agent Toxicity 0.000 description 8
241001465318 Aspergillus terreus Species 0.000 description 6
241000223678 Aureobasidium pullulans Species 0.000 description 6
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
229910052799 carbon Inorganic materials 0.000 description 6
229910052739 hydrogen Inorganic materials 0.000 description 6
239000001257 hydrogen Substances 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
229910052757 nitrogen Inorganic materials 0.000 description 6
229910052717 sulfur Inorganic materials 0.000 description 6
239000011593 sulfur Substances 0.000 description 6
241000221866 Ceratocystis Species 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
241000187481 Mycobacterium phlei Species 0.000 description 5
241000235546 Rhizopus stolonifer Species 0.000 description 5
229940076134 benzene Drugs 0.000 description 5
125000004435 hydrogen atom Chemical class [H]* 0.000 description 5
230000008018 melting Effects 0.000 description 5
238000002844 melting Methods 0.000 description 5
239000000203 mixture Substances 0.000 description 5
229940055036 mycobacterium phlei Drugs 0.000 description 5
239000006916 nutrient agar Substances 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
244000063299 Bacillus subtilis Species 0.000 description 4
235000014469 Bacillus subtilis Nutrition 0.000 description 4
241001557886 Trichoderma sp. Species 0.000 description 4
241000222122 Candida albicans Species 0.000 description 3
229940095731 candida albicans Drugs 0.000 description 3
239000000463 material Substances 0.000 description 3
239000004753 textile Substances 0.000 description 3
241000193830 Bacillus <bacterium> Species 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
244000286779 Hansenula anomala Species 0.000 description 2
235000014683 Hansenula anomala Nutrition 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
241000191967 Staphylococcus aureus Species 0.000 description 2
239000010730 cutting oil Substances 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
239000003292 glue Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000003973 paint Substances 0.000 description 2
239000000123 paper Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
239000000344 soap Substances 0.000 description 2
KKLACKSYGWSSQN-UHFFFAOYSA-N 2,3,6-trichlorobenzenethiol Chemical compound SC1=C(Cl)C=CC(Cl)=C1Cl KKLACKSYGWSSQN-UHFFFAOYSA-N 0.000 description 1
241001123632 Cephaloascus Species 0.000 description 1
UXUCVNXUWOLPRU-UHFFFAOYSA-N Chloromethyl thiocyanate Chemical compound ClCSC#N UXUCVNXUWOLPRU-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 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
208000031888 Mycoses Diseases 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
241000589516 Pseudomonas Species 0.000 description 1
241000191940 Staphylococcus Species 0.000 description 1
241000990222 Tometes Species 0.000 description 1
241001045770 Trichophyton mentagrophytes Species 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
229910001514 alkali metal chloride Inorganic materials 0.000 description 1
125000000217 alkyl group Chemical group 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
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004432 carbon atom Chemical group C* 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
150000003841 chloride salts Chemical class 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
239000000428 dust Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000000295 fuel oil Substances 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000001963 growth medium Substances 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
238000000034 method Methods 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
244000005700 microbiome Species 0.000 description 1
239000004570 mortar (masonry) Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000000575 pesticide 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
239000000843 powder Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007921 spray 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
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C331/00—Derivatives of thiocyanic acid or of isothiocyanic acid
- C07C331/02—Thiocyanates
- C07C331/04—Thiocyanates having sulfur atoms of thiocyanate groups bound to acyclic carbon atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

NO751316A 1974-04-15 1975-04-14 NO751316L (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US46084174A	1974-04-15	1974-04-15

Publications (1)

Publication Number	Publication Date
NO751316L true NO751316L (fr)	1975-10-16

Family

ID=23830281

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO751316A NO751316L (fr)	1974-04-15	1975-04-14

Country Status (7)

Country	Link
JP (1)	JPS50137941A (fr)
CA (1)	CA1027577A (fr)
DE (1)	DE2515699A1 (fr)
ES (1)	ES436373A1 (fr)
GB (1)	GB1476035A (fr)
NL (1)	NL7504112A (fr)
NO (1)	NO751316L (fr)

1975
- 1975-04-07 NL NL7504112A patent/NL7504112A/xx unknown
- 1975-04-07 ES ES436373A patent/ES436373A1/es not_active Expired
- 1975-04-08 CA CA224,065A patent/CA1027577A/fr not_active Expired
- 1975-04-10 JP JP50043859A patent/JPS50137941A/ja active Pending
- 1975-04-10 GB GB1480475A patent/GB1476035A/en not_active Expired
- 1975-04-10 DE DE19752515699 patent/DE2515699A1/de active Pending
- 1975-04-14 NO NO751316A patent/NO751316L/no unknown

Also Published As

Publication number	Publication date
ES436373A1 (es)	1977-01-01
NL7504112A (nl)	1975-10-17
DE2515699A1 (de)	1975-10-23
JPS50137941A (fr)	1975-11-01
GB1476035A (en)	1977-06-10
CA1027577A (fr)	1978-03-07

Publication	Publication Date	Title
DE69518323T2 (de)	2001-02-01	Oxaborole und deren salze, und deren verwendung als biozide
CS235308B2 (en)	1985-05-15	Fungicide and acaracide agent and method of efficient matters production
US3641004A (en)	1972-02-08	Alkyl esters of 6-(benzenesulfonyl)-trihalo-2-picolinic acid
NO751316L (fr)	1975-10-16
US3758482A (en)	1973-09-11	Halopyridyl thiocyanates
US4053633A (en)	1977-10-11	Aryl dibromonitromethyl sulfones
US3712920A (en)	1973-01-23	2,5-thiophenediyl-bis(iodonium salts)
US3787425A (en)	1974-01-22	Halopyridyl thiocyanates
US3787422A (en)	1974-01-22	Halopyridyl thiocyanates
EP0111452A1 (fr)	1984-06-20	Utilisation de pyrroles comme biocides pour la protection des matériaux
US4101546A (en)	1978-07-18	Cyanatothiomethylthio pyrazines
US3549647A (en)	1970-12-22	Bis- and tris-(thio-,sulfinyl- and sulfonyl)pyridines
US3462472A (en)	1969-08-19	1,4- and 1,2-bis(substituted sulfonylthiomethyl)cyclohexane
US3821216A (en)	1974-06-28	Polyhalo-4-pyridine sulfen and sulfonamides
US4035407A (en)	1977-07-12	3,4,5-Trichloro-N,N-di(loweralkyl)-2-thiomethylthiocyanato)benzene-sulfonamides
NO751315L (fr)	1975-10-16
US4041073A (en)	1977-08-09	3,4,5-Trichloro-N,N-di(loweralkyl)-2-(mercapto) benzenesulfonamides
NO751313L (fr)	1975-10-16
US3869466A (en)	1975-03-04	4-cyano-3,5-isothiazolediylbis(thiomethylene)dithiocyanate
NO840421L (no)	1984-08-17	N-sulfenylerte hydantoiner, en fremgangsmaate til deres fremstilling, og deres anvendelse som mikrobizid
US4402980A (en)	1983-09-06	Sulphonic acid cycloalkylamides and their use as microbicides
US2957801A (en)	1960-10-25	Pest control method
US2936262A (en)	1960-05-10	Diels-alder adduct of tetrachloro cyclopentadiene with quinone as a fungicide
US3787500A (en)	1974-01-22	Disubstituted cyclopropenones and method of production
CH631991A5 (de)	1982-09-15	Verfahren zur herstellung von triorganozinnhalogeniden.