THIAMETHOXAM

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C8H10ClN5O3S
Molecular Weight	291.715
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	1
Charge	0

SHOW SMILES / InChI

Structure of THIAMETHOXAM

Structure Search

SMILES

CN1COCN(CC2=CN=C(Cl)S2)\C1=N\[N+]([O-])=O

InChI

InChIKey=NWWZPOKUUAIXIW-DHZHZOJOSA-N

InChI=1S/C8H10ClN5O3S/c1-12-4-17-5-13(8(12)11-14(15)16)3-6-2-10-7(9)18-6/h2H,3-5H2,1H3/b11-8+

HIDE SMILES / InChI

Molecular Formula	C8H10ClN5O3S
Molecular Weight	291.715
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	1
Optical Activity	NONE

Approval Year

PubMed

PubMed

Title	Date	PubMed
Effects of Neonicotinoids on Promoter-Specific Expression and Activity of Aromatase (CYP19) in Human Adrenocortical Carcinoma (H295R) and Primary Umbilical Vein Endothelial (HUVEC) Cells.	2016-01	26464060
Neonicotinoid formaldehyde generators: possible mechanism of mouse-specific hepatotoxicity/hepatocarcinogenicity of thiamethoxam.	2013-02-04	23220038

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:07:41 GMT 2025` Edited by `admin` on `Mon Mar 31 19:07:41 GMT 2025`
Record UNII	747IC8B487
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

(EZ)-3-(2-CHLORO-1,3-THIAZOL-5-YLMETHYL)-5-METHYL-1,3,5-OXADIAZINAN-4-YLIDENE(NITRO)AMINE

Preferred Name

English

THIAMETHOXAM

Common Name

English

3-((2-CHLORO-5-THIAZOLYL)METHYL)TETRAHYDRO-5-METHYL-N-NITRO-4H-1,3,5-OXADIAZIN-4-IMINE

Systematic Name

English

THIAMETHOXAM [MI]

Common Name

English

THIAMETHOXAM [ISO]

Common Name

English

Classification Tree Code System Code

EPA PESTICIDE CODE

60109

Created by admin on Mon Mar 31 19:07:41 GMT 2025 , Edited by admin on Mon Mar 31 19:07:41 GMT 2025

Code System Code Type Description

ALANWOOD

thiamethoxam

Created by admin on Mon Mar 31 19:07:41 GMT 2025 , Edited by admin on Mon Mar 31 19:07:41 GMT 2025

PRIMARY

FDA UNII

747IC8B487

Created by admin on Mon Mar 31 19:07:41 GMT 2025 , Edited by admin on Mon Mar 31 19:07:41 GMT 2025

PRIMARY

HSDB

7938

Created by admin on Mon Mar 31 19:07:41 GMT 2025 , Edited by admin on Mon Mar 31 19:07:41 GMT 2025

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EPA CompTox

DTXSID2034962

Created by admin on Mon Mar 31 19:07:41 GMT 2025 , Edited by admin on Mon Mar 31 19:07:41 GMT 2025

PRIMARY

MERCK INDEX

m10716

Created by admin on Mon Mar 31 19:07:41 GMT 2025 , Edited by admin on Mon Mar 31 19:07:41 GMT 2025

PRIMARY

Merck Index

MESH

C416660

Created by admin on Mon Mar 31 19:07:41 GMT 2025 , Edited by admin on Mon Mar 31 19:07:41 GMT 2025

PRIMARY

CHEBI

39185

Created by admin on Mon Mar 31 19:07:41 GMT 2025 , Edited by admin on Mon Mar 31 19:07:41 GMT 2025

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CAS

153719-23-4

Created by admin on Mon Mar 31 19:07:41 GMT 2025 , Edited by admin on Mon Mar 31 19:07:41 GMT 2025

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PUBCHEM

5821911

Created by admin on Mon Mar 31 19:07:41 GMT 2025 , Edited by admin on Mon Mar 31 19:07:41 GMT 2025

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WIKIPEDIA

THIAMETHOXAM

Created by admin on Mon Mar 31 19:07:41 GMT 2025 , Edited by admin on Mon Mar 31 19:07:41 GMT 2025

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SMS_ID

300000052253

Created by admin on Mon Mar 31 19:07:41 GMT 2025 , Edited by admin on Mon Mar 31 19:07:41 GMT 2025

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Related Record Type Details


					747IC8B487

ACTIVE MOIETY