Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H8S |
| Molecular Weight | 112.193 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(C)S1
InChI
InChIKey=GWQOOADXMVQEFT-UHFFFAOYSA-N
InChI=1S/C6H8S/c1-5-3-4-6(2)7-5/h3-4H,1-2H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| (2E)-3-[4-(Dimethyl-amino)-phen-yl]-1-(2,5-dimethyl-3-thien-yl)prop-2-en-1-one. | 2010-08-25 |
|
| (2E)-1-(2,5-Dimethyl-3-thien-yl)-3-(2-meth-oxy-phen-yl)prop-2-en-1-one. | 2010-08-21 |
|
| (E)-1-(2,5-Dimethyl-3-thien-yl)-3-(2-hy-droxy-phen-yl)prop-2-en-1-one. | 2010-08-11 |
|
| (2E)-3-(3,4-Dimeth-oxy-phen-yl)-1-(2,5-dimethyl-thio-phen-3-yl)prop-2-en-1-one. | 2010-07-31 |
|
| (E)-1-(2,5-Dimethyl-3-thien-yl)-3-(2,4,5-trimeth-oxy-phen-yl)prop-2-en-1-one. | 2010-07-24 |
|
| Effects of selected organo-sulfur compounds on melanin formation. | 2009-08-12 |
|
| Electrogenerated chemiluminescence reaction of tris(2,2'-bipyridine)ruthenium(II) with 2,5-dimethylthiophene as co-reactant in aqueous solution. | 2008-08-01 |
|
| Chemiluminescence detection of five-membered heteroaromatic compounds using electrogenerated tris(2,2'-bipyridine)-ruthenium(III). | 2007-04 |
|
| Aquasonolysis of thiophene and its derivatives. | 2006-01 |
|
| Alleviation of aflatoxin B1-induced oxidative stress in HepG2 cells by volatile extract from Allii Fistulosi Bulbus. | 2005-10-21 |
|
| C-H Bond activation and C-C bond formation in the reaction of 2,5-dimethylthiophene with TpMe2Ir compounds. | 2005-04-21 |
Patents
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Systematic Name | English | ||
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Preferred Name | English | ||
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Code | English |
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638-02-8
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DTXSID2074295
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60689
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211-313-9
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V6DDX6WB12
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12514
Created by
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2,5-Dimethylthiophene
Created by
admin on Mon Mar 31 22:31:50 GMT 2025 , Edited by admin on Mon Mar 31 22:31:50 GMT 2025
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SUBSTANCE RECORD