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5-Methylthiophen-2-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-chloro-5-methylthiophene with water or the condensation of 2-acetylthiophene with hydrogen sulfide. 5-Methylthiophen-2-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.

930-64-3

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930-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 930-64-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 930-64:
(5*9)+(4*3)+(3*0)+(2*6)+(1*4)=73
73 % 10 = 3
So 930-64-3 is a valid CAS Registry Number.

930-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-3H-thiophen-2-one

1.2 Other means of identification

Product number -
Other names 2-Oxo-5-methyl-2.3-dihydro-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:930-64-3 SDS

930-64-3Relevant academic research and scientific papers

Tandem thionation of biomass derived levulinic acid with Lawesson's reagent

Li, Zheng,Tang, Xing,Jiang, Yetao,Zuo, Miao,Wang, Yangjun,Chen, Wei,Zeng, Xianhai,Sun, Yong,Lin, Lu

, p. 2971 - 2975 (2016/06/06)

Herein we report a tandem thionation of biomass derived levulinic acid (LA) to generate thiophenic compounds. LA is initially converted to several thiophenones and then an aromatic di-thionated product, 5-methylthiophene-2-thiol, is obtained with the highest yield of 78%. An overall synthesis of thiophenic products from cellulose is also developed.

Cascade iodination-fluorination synthesis of 2-fluorothiophene and 5-fluoro-2-thienyliodonium salts

Onys'ko, Petro P.,Kim, Tetyana V.,Kiseleva, Olena I.,Rassukana, Yuliya V.,Gakh, Andrei A.

experimental part, p. 501 - 504 (2010/01/14)

The first synthesis of fluorine-containing 2-thienyliodonium salts was accomplished using cascade iodination-fluorination. According to this methodology, thiophene is first converted to bis(2-thienyl)iodonium hexafluorophosphate using an electrophilic iodination reaction. Upon heating with potassium fluoride, this salt undergoes regioselective fluorination producing 2-fluorothiophene. 2-Fluorothiophene is then iodinated again to yield fluorothienyliodonium salts.

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