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2-Methylthiophen-3-ol is an organic compound with the chemical formula C5H6OS. It is a heterocyclic compound, specifically a thiophene derivative, characterized by the presence of a sulfur atom in the ring structure. This colorless liquid has a strong, pungent odor and is soluble in organic solvents. It is synthesized through various methods, including the reaction of 2-methylfuran with hydrogen sulfide or the condensation of 2-methylthiophene with hydroxylamine. 2-Methylthiophen-3-ol is used as a chemical intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a fragrance ingredient in the perfumery industry due to its unique scent profile.

3760-22-3

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3760-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3760-22-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,6 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3760-22:
(6*3)+(5*7)+(4*6)+(3*0)+(2*2)+(1*2)=83
83 % 10 = 3
So 3760-22-3 is a valid CAS Registry Number.

3760-22-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-2-methylthiophene

1.2 Other means of identification

Product number -
Other names 2-Methyl-3-hydroxy-thiophen

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3760-22-3 SDS

3760-22-3Downstream Products

3760-22-3Relevant academic research and scientific papers

Synthesis of 3-hydroxythiophenes and thiophen-3(2H)-ones by pyrolysis of alkylsulfanylmethylene Meldrum's acid derivatives

Hunter, Gordon A.,McNab, Hamish

, p. 1209 - 1214 (2007/10/02)

3-Hydroxythiophene 1 and a range of its 2-substituted, 2,2-disubstituted and 5-substituted derivatives have been made by flash vacuum pyrolysis (FVP) of an appropriate alkylsulfanylmethylene derivative of Meldrum's acid 3 or 4.These compounds are readily obtained, either by reaction of methoxymethylene Meldrum's acid with alkylthiols in refluxing acetonitrile, or via the bis(methylsulfanyl) compound 18 by known procedures.The pyrolysis proceeds by a hydrogen-transfer-cyclisation mechanism in which thereis extensive loss of configuration of a chiral centre at the reaction site.The NMR and mass spectra of the Meldrum's acid precursors and the mass spectra of the 3-hydroxythiophenes are briefly discussed.

Antibacterial penem derivatives

-

, (2008/06/13)

The present invention relates to certain penem derivatives of the general formula I STR1 in which R represents a hydrogen atom or a carboxyl esterifying group, R1 represents certain unsubstituted and substituted aromatic and heterocyclic groups

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