acibenzolar-S-methyl (Q341312)

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chemical compound

S-methyl benzo[d][1,2,3]thiadiazole-7-carbothioate
1,2,3-benzothiadiazole-7-carboxlic acid thiomethyl ester
7-(methylthiocarbonyl)-benzo-1,2,3-thiadiazole
S-methyl benzo[1,2,3]thiadiazole-7-carbothioate
benzo-(1,2,3)-thiadiazole-7-carbothioic acid S-methyl ester
BTH

Language	Label	Description	Also known as
English	acibenzolar-S-methyl	chemical compound	S-methyl benzo[d][1,2,3]thiadiazole-7-carbothioate 1,2,3-benzothiadiazole-7-carboxlic acid thiomethyl ester 7-(methylthiocarbonyl)-benzo-1,2,3-thiadiazole S-methyl benzo[1,2,3]thiadiazole-7-carbothioate benzo-(1,2,3)-thiadiazole-7-carbothioic acid S-methyl ester BTH

Statements

type of chemical entity

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chemical compound

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chemical structure

Acibenzolar-S-methyl .png
850 × 489; 12 KB

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imported from Wikimedia project

German Wikipedia

image of molecular model or crystal lattice model

Acibenzolar-S-methyl-3D-spacefill.png
1,560 × 2,000; 540 KB

space-filling model

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209.992 dalton

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language of work or name

Acibenzolar-S-Methyl (English)

7 October 2016

chemical formula

C₈H₆N₂OS₂

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language of work or name

Acibenzolar-S-Methyl (English)

20 November 2016

canonical SMILES

CSC(=O)C1=C2C(=CC=C1)N=NS2

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language of work or name

Acibenzolar-S-Methyl (English)

20 November 2016

Arabidopsis thaliana

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Overexpression of salicylic acid carboxyl methyltransferase reduces salicylic acid-mediated pathogen resistance in Arabidopsis thaliana.

Phaseolus vulgaris

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Effect of salicylic acid and structurally related compounds in the accumulation of phytoalexins in cotyledons of common bean (Phaseolus vulgaris L.) cultivars

Commons category

Acibenzolar-S-methyl

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Identifiers

InChI=1S/C8H6N2OS2/c1-12-8(11)5-3-2-4-6-7(5)13-10-9-6/h2-4H,1H3

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language of work or name

Acibenzolar-S-Methyl (English)

20 November 2016

UELITFHSCLAHKR-UHFFFAOYSA-N

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language of work or name

Acibenzolar-S-Methyl (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

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Global Substance Registration System

language of work or name

acibenzolar-S-methyl (English)

20 November 2016

CAS Common Chemistry

7 April 2021

https://commonchemistry.cas.org/detail?cas_rn=135158-54-2

UELITFHSCLAHKR-UHFFFAOYSA-N

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language of work or name

acibenzolar-S-methyl (English)

7 October 2016

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language of work or name

Acibenzolar-S-Methyl (English)

20 November 2016

Reaxys registry number

8055445

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language of work or name

acibenzolar-S-methyl (English)

7 October 2016

mapping relation type

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language of work or name

ACIBENZOLAR-S-METHYL (English)

20 November 2016

1 reference

language of work or name

ACIBENZOLAR-S-METHYL (English)

20 November 2016

UniChem compound ID

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splash10-03di-1290000000-6900733e9653e31eb576

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splash10-01p9-1940000000-ce88e29d45444eaf810b

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1 reference

imported from Wikimedia project

German Wikipedia

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Hazardous Substances Data Bank

publication date

28 October 2019

ACIBENZOLAR-S-METHYL (English)

10 May 2021

DSSTox substance ID

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Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

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420-050-0

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ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

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

CAS no.: 135158-54-2 (English)

ECHA Substance Infocard ID

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http://echa.europa.eu/de/information-on-chemicals/registered-substances

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Global Substance Registration System

language of work or name

acibenzolar-S-methyl (English)

20 November 2016

Probes And Drugs ID

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1 reference

Freebase Data Dumps

publication date

28 October 2013

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Microsoft Academic ID

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Römpp online ID

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imported from Wikimedia project

German Wikipedia

Sitelinks

Wikipedia(10 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(1 entry)

commonswiki Category:Acibenzolar-S-methyl

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