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S-methyl benzo(1.2.3)thiadiazole-7-carbothioate

CAS 135158-54-2C8H6N2OS2MW 210.3

S-methyl benzo(1.2.3)thiadiazole-7-carbothioate (CAS 135158-54-2) — formula C8H6N2OS2, molecular weight 210.3; category organic chemicals.

Product Overview

CAS Number135158-54-2
Molecular FormulaC8H6N2OS2
Molecular Weight210.3
Melting Point132.9 °C
Boiling PointApprox 267 °C
LogPlog Kow = 3.1 @ 25 °C
ApplicationsUses: Used to protect crops by activating the natural response to disease (systemic acquired resistance), [Merck Index] Used to control downy mildew in vegetables, bacterial speck and spot on tomatoes, and blue mold on tobacco, One end use product used on imported bananas, [Reference #1], Farming (Pesticides) [Category: Industry], For Acibenzolar-S-methyl (USEPA, OPP Pesticide Code: 061402) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., No residential uses, are, either registered or pending., Plant activator ... activates the plants natural defense mechanism, Used to control a range of diseases in wheat and it is being developed for use in rice, bananas, vegetables and tobacco., This is a man-made compound that is used as a pesticide., Use Classification: Environmental transformation -> Pesticides (parent, predecessor), Plant activators, Fungicides, Insecticides, Methods of Manufacturing: Prepn: R. Schurter et al., EP 313512, eidem US 5523311 (1989, 1996 both to Ciba-Geigy)., Formulations, Preparations: Water dispersible granules, 50% active ingredient
CategoryOrganic Chemicals

Applications

Documented applications: Uses: Used to protect crops by activating the natural response to disease (systemic acquired resistance), [Merck Index] Used to control downy mildew in vegetables, bacterial speck and spot on tomatoes, and blue mold on tobacco, One end use product used on imported bananas, [Reference #1], Farming (Pesticides) [Category: Industry], For Acibenzolar-S-methyl (USEPA, OPP Pesticide Code: 061402) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., No residential uses, are, either registered or pending., Plant activator ... activates the plants natural defense mechanism, Used to control a range of diseases in wheat and it is being developed for use in rice, bananas, vegetables and tobacco., This is a man-made compound that is used as a pesticide., Use Classification: Environmental transformation -> Pesticides (parent, predecessor), Plant activators, Fungicides, Insecticides, Methods of Manufacturing: Prepn: R. Schurter et al., EP 313512, eidem US 5523311 (1989, 1996 both to Ciba-Geigy)., Formulations, Preparations: Water dispersible granules, 50% active ingredient.

Technical Profile

What this product is

S-methyl benzo(1.2.3)thiadiazole-7-carbothioate is a carbon-based organic compound with CAS registry number 135158-54-2 and molecular formula C8H6N2OS2 (molecular weight 210.3), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 135158-54-2

Its molecular formula C8H6N2OS2 comprises 8 C, 6 H, 2 N, 1 O, 2 S atoms.

Also known as: S-methyl benzo(1.2.3)thiadiazole-7-carbothioate · S-甲基苯并(1.2.3)噻二唑-7-硫代甲酸酯

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of S-methyl benzo(1.2.3)thiadiazole-7-carbothioate?

The CAS registry number of S-methyl benzo(1.2.3)thiadiazole-7-carbothioate is 135158-54-2.

What is the molecular formula and molecular weight of S-methyl benzo(1.2.3)thiadiazole-7-carbothioate?

Molecular formula C8H6N2OS2, molecular weight 210.3.

What other names is S-methyl benzo(1.2.3)thiadiazole-7-carbothioate known by?

It is also registered under: S-methyl benzo(1.2.3)thiadiazole-7-carbothioate, S-甲基苯并(1.2.3)噻二唑-7-硫代甲酸酯.

What are the documented applications of S-methyl benzo(1.2.3)thiadiazole-7-carbothioate?

Recorded applications: Uses: Used to protect crops by activating the natural response to disease (systemic acquired resistance), [Merck Index] Used to control downy mildew in vegetables, bacterial speck and spot on tomatoes, and blue mold on tobacco, One end use product used on imported bananas, [Reference #1], Farming (Pesticides) [Category: Industry], For Acibenzolar-S-methyl (USEPA, OPP Pesticide Code: 061402) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., No residential uses, are, either registered or pending., Plant activator ... activates the plants natural defense mechanism, Used to control a range of diseases in wheat and it is being developed for use in rice, bananas, vegetables and tobacco., This is a man-made compound that is used as a pesticide., Use Classification: Environmental transformation -> Pesticides (parent, predecessor), Plant activators, Fungicides, Insecticides, Methods of Manufacturing: Prepn: R. Schurter et al., EP 313512, eidem US 5523311 (1989, 1996 both to Ciba-Geigy)., Formulations, Preparations: Water dispersible granules, 50% active ingredient.

Which category does S-methyl benzo(1.2.3)thiadiazole-7-carbothioate belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for S-methyl benzo(1.2.3)thiadiazole-7-carbothioate (CAS 135158-54-2), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number135158-54-2
PubChem CID86412
Molecular formulaC8H6N2OS2
IUPAC nameS-methyl 1,2,3-benzothiadiazole-7-carbothioate
UNII (FDA)BCW6119347

Computed descriptors

Molecular Weight210.3
XLogP32.3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count5
Rotatable Bond Count2
Exact Mass209.99215517
Monoisotopic Mass209.99215517
Topological Polar Surface Area96.4
Heavy Atom Count13

Physicochemical values on record

Boiling PointApprox 267 °C
Melting Point132.9 °C
SolubilityIn water, 7.7 mg/l @ 25 °C
Density1.54X10+3 g/cu cm @ 22 °C
Vapor Pressure0.0000033 [mmHg]
Vapor Pressure3.30X10-6 mm Hg @ 25 °C
LogPlog Kow = 3.1 @ 25 °C
Formulations/Preparations50% active ingredient

Documented uses on record

    Used to protect crops by activating the natural response to disease (systemic acquired resistance); [Merck Index] Used to control downy mildew in vegetables, bacterial speck and spot on tomatoes, and blue mold on tobacco; One end use product used on imported bananas; [Reference #1]No residential uses /are/ either registered or pending.

    Synonyms and trade names

    Acibenzolar-S-Methyl; 135158-54-2; Actigard; S-Methyl 1,2,3-benzothiadiazole-7-carbothioate; Bendicar; Bion (pesticide); BTH (agrochemical); DTXSID1032519; CGA 245704; 7-(methylthiocarbonyl)-benzo-1,2,3-thiadiazole; BCW6119347; GGA 245704; DTXCID9012519; CHEBI:73178; s-methyl benzo(1,2,3)thiadiazole-7-carbothioate; 1,2,3-benzothiadiazole-7-carboxlic acid thiomethyl ester

    GHS hazard classification

    Reported hazard statementsH315, H317, H319, H335, H400, H410

    H315: Causes skin irritation [Warning Skin corrosion/irritation]

    H317: May cause an allergic skin reaction [Warning Sensitization, Skin]

    What the public record says

    S-methyl benzo(1.2.3)thiadiazole-7-carbothioate · CAS 135158-54-2 · C8H6N2OS2. UNII BCW6119347. Boiling Point: Approx 267 °C; Melting Point: 132.9 °C; Solubility: In water, 7.7 mg/l @ 25 °C.

    Physical description and handling notes

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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