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1132832-80-4

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1132832-80-4 Usage

General Description

2-Fluoro-5-(thiophen-2-yl)pyridine is a chemical compound with the molecular formula C9H6FN2S. It is a fluorinated pyridine derivative with a thiophene group attached to the 5-position of the pyridine ring. 2-fluoro-5-(thiophen-2-yl)pyridine is used in pharmaceutical and agrochemical research and development, as well as in the production of specialty chemicals. It exhibits potential biological activity and is a valuable building block for the synthesis of various heterocyclic compounds. Its unique structure and properties make it a valuable and versatile tool in chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1132832-80-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,2,8,3 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1132832-80:
(9*1)+(8*1)+(7*3)+(6*2)+(5*8)+(4*3)+(3*2)+(2*8)+(1*0)=124
124 % 10 = 4
So 1132832-80-4 is a valid CAS Registry Number.

1132832-80-4SDS

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 2-fluoro-5-thiophen-2-ylpyridine

1.2 Other means of identification

Product number -
Other names 2-fluoro-5-(thiophen-2-yl)pyridine

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:1132832-80-4 SDS

1132832-80-4Relevant articles and documents

A modified procedure for the palladium catalyzed borylation/Suzuki-Miyaura cross-coupling of aryl and heteroaryl halides utilizing bis-boronic acid

Molander, Gary A.,Trice, Sarah L.J.,Tschaen, Brittany

, p. 5758 - 5764 (2015)

Abstract A modified Pd-catalyzed method of forming aryl- and heteroarylboron species and a two-step, one-pot borylation/Suzuki-Miyaura cross coupling using the atom economical tetrahydroxydiboron (bis-boronic acid, BBA) is reported. By using ethylene glycol as an additive, the new method results in increased yields, lower BBA loading, faster reaction times, and a broader reaction scope, including previously problematic substrates such as heterocycles.

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