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139163-64-7

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139163-64-7 Usage

Description

(1R)-1-(6-Bromopyridin-3-yl)ethan-1-ol is a chemical compound that belongs to the class of alcohols. It is composed of a 1R stereoisomer, a 6-bromopyridin-3-yl moiety, and an ethan-1-ol functional group. (1R)-1-(6-Bromopyridin-3-yl)ethan-1-ol is characterized by its specific properties, such as solubility, melting point, and boiling point, which make it suitable for a range of applications in the chemical industry.

Uses

Used in Organic Synthesis:
(1R)-1-(6-Bromopyridin-3-yl)ethan-1-ol is used as a reagent in organic synthesis for the preparation of various chemical compounds. Its unique structure and functional groups allow it to participate in a variety of chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical and Agrochemical Production:
(1R)-1-(6-Bromopyridin-3-yl)ethan-1-ol serves as a building block for the production of various pharmaceuticals and agrochemicals. Its incorporation into these products can contribute to their efficacy, stability, and other desired properties.
Used in Chemical Industry:
Due to its specific properties, (1R)-1-(6-Bromopyridin-3-yl)ethan-1-ol is also used in the chemical industry for a range of applications. These may include its use as a solvent, a reactant in chemical processes, or as an intermediate in the synthesis of other compounds.
Potential Use in Drug Discovery and Development:
(1R)-1-(6-Bromopyridin-3-yl)ethan-1-ol may also possess biological activities or pharmacological effects that could be of interest in drug discovery and development. Its unique structure and functional groups could potentially be harnessed to create new drugs or improve existing ones, making it a promising candidate for further research in this field.

Check Digit Verification of cas no

The CAS Registry Mumber 139163-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,1,6 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 139163-64:
(8*1)+(7*3)+(6*9)+(5*1)+(4*6)+(3*3)+(2*6)+(1*4)=137
137 % 10 = 7
So 139163-64-7 is a valid CAS Registry Number.

139163-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name R-(6-bromopyridin-3-yl)ethanol

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:139163-64-7 SDS

139163-64-7Downstream Products

139163-64-7Relevant articles and documents

Enantioselective Synthesis of Optically Active Pyridine Derivatives and C2-Symmetric 2,2'-Bipyridines

Bolm, Carsten,Ewald, Martina,Felder, Marcel,Schlingloff, Gunther

, p. 1169 - 1190 (2007/10/02)

Optically active pyridine derivatives 2, 15, 18, 19, 21, 26, and 27 are obtained by enantioselective reduction of the corresponding ketones 5, 7, 11-13, 24, and 25 using the chiral borane reagent chlorodiisopinocampherylborane .Nickel(0)-mediated coupling of bromopyridines 2, 15, and 31 gives C2-symmetric 2,2'-bipyridines (R,R)-32, (R,R)-33, and (S,S)-38, respectively, which form metal complexex with Co(II), Pd(II), Cu(I), and Ag(I).Aryl-substituted pyridines 26, and 39-41 are synthesized by palladium(0)-catalized cross coupling of 2 and 15 with boronic acids 42-44.Key Words: 2,2-Bipyridines / Pyridines, optically active / Chiral ligands / Asymmetric Synthesis / Catalysis, enantioselective

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