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Details

Stereochemistry ACHIRAL
Molecular Formula C7H6N2S
Molecular Weight 150.201
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-BENZIMIDAZOLETHIOL

SMILES

SC1=NC2=C(N1)C=CC=C2

InChI

InChIKey=YHMYGUUIMTVXNW-UHFFFAOYSA-N
InChI=1S/C7H6N2S/c10-7-8-5-3-1-2-4-6(5)9-7/h1-4H,(H2,8,9,10)

HIDE SMILES / InChI

Molecular Formula C7H6N2S
Molecular Weight 150.201
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Transformation of BALB/c-3T3 cells: IV. Rank-ordered potency of 24 chemical responses detected in a sensitive new assay procedure.
1993 Jul
Determination of very low levels of dissolved mercury(II) and methylmercury in river waters by continuous flow with on-line UV decomposition and cold-vapor atomic fluorescence spectrometry after pre-concentration on a silica gel-2-mercaptobenzimidazol sorbent.
2001 Dec 24
Differential pulse adsorption stripping voltammetric determination of copper(II) with 2-mercaptobenzimidazol at a hanging mercury-drop electrode.
2001 May
Removal of mercury(II) from aqueous solutions and chlor-alkali industry wastewater using 2-mercaptobenzimidazole-clay.
2002 Mar
Square wave voltammetric sensing of uric acid using the self-assembly of mercaptobenzimidazole.
2002 Sep
Potent mammalian cerebroprotection and neuronal cell death inhibition are afforded by a synthetic antioxidant analogue of marine invertebrate cell protectant ovothiols.
2003 Sep
High-throughput microplate phosphorylation assays based on DevR-DevS/Rv2027c 2-component signal transduction pathway to screen for novel antitubercular compounds.
2005 Apr
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005 Jun
Domino Michael addition-carbene rearrangement-cyclization reaction of 1-alkynyl(aryl)-lambda3-bromanes with 2-mercapto-1,3-benzazoles.
2005 Oct 28
Interaction of thioamides, selenoamides, and amides with diiodine.
2006
Reactions Between Chalcogen Donors and Dihalogens/Interalogens: Typology of Products and Their Characterization by FT-Raman Spectroscopy.
2006
Bioinorganic chemistry in thyroid gland: effect of antithyroid drugs on peroxidase-catalyzed oxidation and iodination reactions.
2006
Green route for the heterocyclization of 2-mercaptobenzimidazole into beta-lactum segment derivatives containing -CONH- bridge with benzimidazole: Screening in vitro antimicrobial activity with various microorganisms.
2006 Dec 15
Parallel synthesis of 2-sulphanylated bis-benzimidazoles on soluble polymer support.
2008 May-Jun
[Specific effects of selective anxiolytic afobazole on the cardiovascular system].
2009 Jan-Feb
Determination of thyreostats in urine and thyroid gland by ultra high performance liquid chromatography tandem mass spectrometry.
2009 Nov 13
2,2'-Bis(methyl-ene)-3,3'-(2-thioxo-2,3-dihydro-1H-benzimidazole-1,3-di-yl)dipropane-nitrile.
2009 Oct 31
Simultaneous spectrophotometric determination of 2-thiouracil and 2-mercaptobenzimidazole in animal tissue using multivariate calibration methods: concerns and rapid methods for detection.
2010 Mar
3-[2-(1H-Benzimidazol-2-ylsulfan-yl)eth-yl]-1,3-oxazolidin-2-one.
2010 Nov 13
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:12:21 GMT 2025
Edited
by admin
on Mon Mar 31 19:12:21 GMT 2025
Record UNII
619CVM6HOK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-BENZIMIDAZOLETHIOL
MI  
Systematic Name English
RABEPRAZOLE RELATED COMPOUND C
USP-RS  
Preferred Name English
NSC-21414
Code English
MERCAPTOBENZIMIDAZOLE [USP IMPURITY]
Common Name English
MERCAPTOBENZIMIDAZOLE
Common Name English
2-MERCAPTOBENZIMIDAZOLE
Systematic Name English
MERCAPTOBENZIMIDAZOLE, 2-
Systematic Name English
NSC-186246
Code English
RABEPRAZOLE RELATED COMPOUND C [USP IMPURITY]
Common Name English
RABEPRAZOLE SODIUM IMPURITY F [EP IMPURITY]
Common Name English
NCI-C60980
Code English
1H-BENZIMIDAZOLE-2-THIOL
Systematic Name English
2-BENZIMIDAZOLETHIOL [MI]
Common Name English
RABEPRAZOLE RELATED COMPOUND C [USP-RS]
Common Name English
2H-BENZIMIDAZOLE-2-THIONE, 1,3-DIHYDRO-
Systematic Name English
NCI-C56268
Code English
LANSOPRAZOLE IMPURITY E [EP IMPURITY]
Common Name English
1,3-DIHYDRO-2H-BENZIMIDAZOLE-2-THIONE
Systematic Name English
Code System Code Type Description
WIKIPEDIA
Mercaptobenzimidazole
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
PRIMARY
MESH
C030698
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
PRIMARY
PUBCHEM
707035
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
PRIMARY
MERCK INDEX
m2354
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
PRIMARY Merck Index
NSC
186246
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
PRIMARY
NSC
21414
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-502-6
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
PRIMARY
SMS_ID
300000052996
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
PRIMARY
FDA UNII
619CVM6HOK
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
PRIMARY
CAS
134469-07-1
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
ALTERNATIVE
RS_ITEM_NUM
1598042
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
PRIMARY
CAS
583-39-1
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
PRIMARY
EPA CompTox
DTXSID9025536
Created by admin on Mon Mar 31 19:12:22 GMT 2025 , Edited by admin on Mon Mar 31 19:12:22 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
PARENT -> IMPURITY
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP