SK277947B6 - 2-(4-chlorobenzothiazolyl)-2-(4-chlorobenzothiazol) carbadithioate - Google Patents

2-(4-chlorobenzothiazolyl)-2-(4-chlorobenzothiazol) carbadithioate Download PDF

Info

Publication number: SK277947B6
Authority: SK; Slovakia
Prior art keywords: chlorobenzothiazolyl; carbadithioate; chlorobenzothiazol; compound; dichlorobenzothiazole
Prior art date: 1990-04-02

Application number

SK160590A

Other languages

English (en)

Slovak (sk)

Inventor

Margita Lacova

Ester Ticha

Stefan Varkonda

Vaclav Konecny

Original Assignee

Margita Lacova

Ester Ticha

Stefan Varkonda

Vaclav Konecny

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.)

1990-04-02

Filing date

1990-04-02

Publication date

1995-09-13

1990-04-02 Application filed by Margita Lacova, Ester Ticha, Stefan Varkonda, Vaclav Konecny filed Critical Margita Lacova

1995-09-13 Publication of SK277947B6 publication Critical patent/SK277947B6/sk

Links

150000001875 compounds Chemical class 0.000 claims abstract description 9
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims abstract description 8
JJWANONAOYNRME-UHFFFAOYSA-N 2,4-dichloro-1,3-benzothiazole Chemical compound C1=CC=C2SC(Cl)=NC2=C1Cl JJWANONAOYNRME-UHFFFAOYSA-N 0.000 claims abstract description 4
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 claims description 6
-1 Chlorobenzothiazolyl Chemical group 0.000 claims description 5
238000000034 method Methods 0.000 claims description 5
IFEPGHPDQJOYGG-UHFFFAOYSA-N 4-chloro-1,3-benzothiazole Chemical compound ClC1=CC=CC2=C1N=CS2 IFEPGHPDQJOYGG-UHFFFAOYSA-N 0.000 claims description 4
239000000203 mixture Substances 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
230000000855 fungicidal effect Effects 0.000 abstract description 4
241000123650 Botrytis cinerea Species 0.000 abstract description 2
241001459558 Monographella nivalis Species 0.000 abstract description 2
230000015572 biosynthetic process Effects 0.000 abstract description 2
238000006243 chemical reaction Methods 0.000 abstract description 2
238000003786 synthesis reaction Methods 0.000 abstract description 2
229910052739 hydrogen Inorganic materials 0.000 abstract 2
239000001257 hydrogen Substances 0.000 abstract 2
125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
241000223600 Alternaria Species 0.000 abstract 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
239000007864 aqueous solution Substances 0.000 abstract 1
229910052799 carbon Inorganic materials 0.000 abstract 1
229910052708 sodium Inorganic materials 0.000 abstract 1
239000011734 sodium Substances 0.000 abstract 1
230000000843 anti-fungal effect Effects 0.000 description 3
239000012141 concentrate Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
238000012360 testing method Methods 0.000 description 2
QJQZRLXDLORINA-UHFFFAOYSA-N 2-cyclohexylethanol Chemical compound OCCC1CCCCC1 QJQZRLXDLORINA-UHFFFAOYSA-N 0.000 description 1
BIHPYCDDPGNWQO-UHFFFAOYSA-N 5-iai Chemical compound C1=C(I)C=C2CC(N)CC2=C1 BIHPYCDDPGNWQO-UHFFFAOYSA-N 0.000 description 1
DTCJYIIKPVRVDD-UHFFFAOYSA-N Benzthiazuron Chemical compound C1=CC=C2SC(NC(=O)NC)=NC2=C1 DTCJYIIKPVRVDD-UHFFFAOYSA-N 0.000 description 1
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
230000003750 conditioning effect Effects 0.000 description 1
150000002023 dithiocarboxylic acids Chemical class 0.000 description 1
229940079593 drug Drugs 0.000 description 1
239000003814 drug Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
244000053095 fungal pathogen Species 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
238000000338 in vitro Methods 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
238000005259 measurement Methods 0.000 description 1
239000002609 medium Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000012544 monitoring process Methods 0.000 description 1
239000006916 nutrient agar Substances 0.000 description 1
244000052769 pathogen Species 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000012216 screening Methods 0.000 description 1
239000002689 soil Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000009466 transformation Effects 0.000 description 1
238000000844 transformation Methods 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)

SK160590A 1990-04-02 1990-04-02 2-(4-chlorobenzothiazolyl)-2-(4-chlorobenzothiazol) carbadithioate SK277947B6 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CS901605A CS160590A2 (en)	1990-04-02	1990-04-02	2-(chlorobenzothiazolyl)-2-(4-chlorobenzothiazole carbadithioate

Publications (1)

Publication Number	Publication Date
SK277947B6 true SK277947B6 (en)	1995-09-13

Family

ID=5350843

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK160590A SK277947B6 (en)	1990-04-02	1990-04-02	2-(4-chlorobenzothiazolyl)-2-(4-chlorobenzothiazol) carbadithioate

Country Status (2)

Country	Link
CS (1)	CS160590A2 (cs)
SK (1)	SK277947B6 (cs)

1990
- 1990-04-02 SK SK160590A patent/SK277947B6/sk unknown
- 1990-04-02 CS CS901605A patent/CS160590A2/cs unknown

Also Published As

Publication number	Publication date
CS160590A2 (en)	1991-10-15

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