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Details

Stereochemistry ACHIRAL
Molecular Formula C5H6S
Molecular Weight 98.166
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-METHYLTHIOPHENE

SMILES

CC1=CC=CS1

InChI

InChIKey=XQQBUAPQHNYYRS-UHFFFAOYSA-N
InChI=1S/C5H6S/c1-5-3-2-4-6-5/h2-4H,1H3

HIDE SMILES / InChI

Molecular Formula C5H6S
Molecular Weight 98.166
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Diethyl 5-acetamido-3-methyl-thio-phene-2,4-dicarboxyl-ate.
2010-11-13
On-line measurement of oxidative degradation kinetics for trace gasoline contaminants in aqueous solutions and natural water by membrane introduction tandem mass spectrometry.
2010-11
Polymer-bound oxidovanadium(IV) and dioxidovanadium(V) complexes as catalysts for the oxidative desulfurization of model fuel diesel.
2010-07-19
Origin and distribution of thiophenes and furans in gas discharges from active volcanoes and geothermal systems.
2010-03-31
Diastereoselective domino reactions of chiral 2-substituted 1-(2',2',3',3'-tetramethylcyclopropyl)-alkan-1-ols under Friedel-Crafts conditions.
2009-07-03
N-[(E)-(5-Methyl-thio-phen-2-yl)methyl-idene]-1H-1,2,4-triazol-3-amine.
2008-12-13
Selectivity in the oxidative addition of C-S bonds of substituted thiophenes to the (C5Me5)Rh(PMe3) fragment: a comparison of theory with experiment.
2008-12-01
Methylated DNA recognition during the reversal of epigenetic silencing is regulated by cysteine and serine residues in the Epstein-Barr virus lytic switch protein.
2008-03-07
Highly diastereoselective Friedel-Crafts alkylation reactions via chiral alpha-functionalized benzylic carbocations.
2008-02-01
Quinoline synthesis: scope and regiochemistry of photocyclisation of substituted benzylidenecyclopentanone O-alkyl and O-acetyloximes.
2007-12-07
MGMT inhibitors--The Trinity College-Paterson Institute experience, a chemist's perception.
2007-08-01
Chemoenzymatic formation of novel aminocoumarin antibiotics by the enzymes CouN1 and CouN7.
2007-07-17
[Determination and distribution of sulfur compounds in coked gasoline by gas chromatography-sulfur chemiluminescence detection].
2007-05
Aquasonolysis of thiophene and its derivatives.
2006-01
Adsorption, desorption, and conversion of thiophene on H-ZSM5.
2004-12-07
[Determination of sulfur compounds in fluid catalytic cracking gasoline by gas chromatography with a sulfur chemiluminescence detector].
2004-05
Aroma extract dilution analysis of Cv. Marion (Rubus spp. hyb) and Cv. Evergreen (R. laciniatus L.) blackberries.
2003-05-21
Thiophenes as traps for benzyne. 3. Diaryl sulfides and the role of dipolar intermediates.
2003-01-10
One-pot synthesis of C-glycosylic compounds (C-glycosides) from D-glucal, p-tolylsulfenyl chloride and aromatic/heteroaromatic compounds in the presence of Lewis acids.
2002-08-16
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:35:26 GMT 2025
Edited
by admin
on Mon Mar 31 20:35:26 GMT 2025
Record UNII
7115JAP77A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEMA NO. 4928
Preferred Name English
2-METHYLTHIOPHENE
Systematic Name English
THIOPHENE, 2-METHYL-
Systematic Name English
.ALPHA.-METHYLTHIOPHENE
Common Name English
Code System Code Type Description
CAS
554-14-3
Created by admin on Mon Mar 31 20:35:26 GMT 2025 , Edited by admin on Mon Mar 31 20:35:26 GMT 2025
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FDA UNII
7115JAP77A
Created by admin on Mon Mar 31 20:35:26 GMT 2025 , Edited by admin on Mon Mar 31 20:35:26 GMT 2025
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CHEBI
141567
Created by admin on Mon Mar 31 20:35:26 GMT 2025 , Edited by admin on Mon Mar 31 20:35:26 GMT 2025
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EPA CompTox
DTXSID3060291
Created by admin on Mon Mar 31 20:35:26 GMT 2025 , Edited by admin on Mon Mar 31 20:35:26 GMT 2025
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ECHA (EC/EINECS)
209-063-0
Created by admin on Mon Mar 31 20:35:26 GMT 2025 , Edited by admin on Mon Mar 31 20:35:26 GMT 2025
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PUBCHEM
11126
Created by admin on Mon Mar 31 20:35:26 GMT 2025 , Edited by admin on Mon Mar 31 20:35:26 GMT 2025
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WIKIPEDIA
2-Methylthiophene
Created by admin on Mon Mar 31 20:35:26 GMT 2025 , Edited by admin on Mon Mar 31 20:35:26 GMT 2025
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