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139342-11-3

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139342-11-3 Usage

Appearance

White to off-white solid

Usage

Building block in organic synthesis

Chemical classification

Derivative of pyridine

Pyridine structure

Six-membered heterocyclic compound with a nitrogen atom in the ring

Industry applications

Pharmaceutical industry, synthesis of various organic compounds

Additional uses

Reagent in chemical reactions, intermediate in the production of other chemicals

Potential applications

Development of new drugs, agrochemicals, and industrial materials

Check Digit Verification of cas no

The CAS Registry Mumber 139342-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,3,4 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 139342-11:
(8*1)+(7*3)+(6*9)+(5*3)+(4*4)+(3*2)+(2*1)+(1*1)=123
123 % 10 = 3
So 139342-11-3 is a valid CAS Registry Number.

139342-11-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-1-(2-bromopyridin-6-yl)propanol

1.2 Other means of identification

Product number -
Other names -

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:139342-11-3 SDS

139342-11-3Downstream Products

139342-11-3Relevant articles and documents

Catalyzed Enantioselective Alkylation of Aldehydes

Bolm, Carsten,Schlingloff, Gunther,Harms, Klaus

, p. 1191 - 1204 (2007/10/02)

Enantioselective alkylation of a variety of aldehydes with diethylzinc was achieved by using catalytic amounts of optically active pyridines and C2-symmetric 2,2'-bipyridines.The products were obtained in good yields with high enantioselectivit

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