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1481-00-1

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1481-00-1 Usage

General Description

2-Fluoro-5-methylthiophene is a chemical compound with the molecular formula C5H5FS. It is a colorless liquid with a strong, unpleasant odor. This chemical is mainly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a solvent in various chemical reactions. 2-Fluoro-5-methylthiophene is considered to be a hazardous chemical and should be handled with care due to its toxicity and potential for environmental harm.

Check Digit Verification of cas no

The CAS Registry Mumber 1481-00-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1481-00:
(6*1)+(5*4)+(4*8)+(3*1)+(2*0)+(1*0)=61
61 % 10 = 1
So 1481-00-1 is a valid CAS Registry Number.

1481-00-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-5-methylthiophene

1.2 Other means of identification

Product number -
Other names 2-Fluor-5-methyl-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:1481-00-1 SDS

1481-00-1Downstream Products

1481-00-1Relevant articles and documents

Decarboxylative Fluorination of Electron-Rich Heteroaromatic Carboxylic Acids with Selectfluor

Yuan, Xi,Yao, Jian-Fei,Tang, Zhen-Yu

supporting information, p. 1410 - 1413 (2017/03/23)

A transition-metal-free decarboxylative fluorination of electron-rich five-membered heteroaromatics, including furan-, pyrazole-, isoxazole-, thiophene-, indole-, benzofuran- and indazolecarboxylic acids, with Selectfluor is reported. Fluorinated dimer products were observed for nitrogen-containing heteroaromatic carboxylic acids, such as indole and pyrazole. An effective method has been developed to synthesize the monomer of 2- and 3-fluoroindoles with Li2CO3 as base at low temperature.

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