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201863-99-2

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201863-99-2 Usage

General Description

"(R)-b-AMino-4-chlorobenzenepropanol" is a chemical compound with a molecular formula C9H12ClNO. It is a chiral compound with a specific stereochemistry configuration. (R)-b-AMino-4-chlorobenzenepropanol is derived from benzene and propanol, and it contains an amino group and a chlorobenzene group. It may be used in organic synthesis or as a building block for the production of pharmaceuticals or other chemical compounds. Its specific properties and potential applications would depend on its stereochemistry and other structural characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 201863-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,8,6 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 201863-99:
(8*2)+(7*0)+(6*1)+(5*8)+(4*6)+(3*3)+(2*9)+(1*9)=122
122 % 10 = 2
So 201863-99-2 is a valid CAS Registry Number.

201863-99-2SDS

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 (R)-2-amino-3-(4-chlorophenyl)propan-1-ol

1.2 Other means of identification

Product number -
Other names (R)-b-Amino-4-chlorobenzenepropanol

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:201863-99-2 SDS

201863-99-2Downstream Products

201863-99-2Relevant articles and documents

Electronic effects of aryl-substituted bis(oxazoline) ligands on the outcome of asymmetric copper-catalysed C-H insertion and aromatic addition reactions

Slattery, Catherine N.,O'Keeffe, Sarah,Maguire, Anita R.

, p. 1265 - 1275 (2013/11/19)

The effect of the modification of bis(oxazoline) ligands on the outcome of copper-catalysed C-H insertion and aromatic addition reactions is described. In general, these reactions display minimum sensitivity in terms of enantiocontrol to variation of the electronic properties of the aryl moiety of the ligand however, some influence is observed for C-H insertions employing naphthyl-substituted bis(oxazolines) and for aromatic addition reactions of biphenyl diazo ketone substrates. The synthesis of the modified bis(oxazolines), which include four novel structures, is also described.

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