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(S)-(+)-2-AMINO-1-PHENYLETHANOL HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71025-82-6

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71025-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71025-82-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,2 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71025-82:
(7*7)+(6*1)+(5*0)+(4*2)+(3*5)+(2*8)+(1*2)=96
96 % 10 = 6
So 71025-82-6 is a valid CAS Registry Number.

71025-82-6SDS

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 (S)-2-amino-1-phenyl-ethanol, hydrochloride

1.2 Other means of identification

Product number -
Other names (S)-2-Amino-1-phenyl-aethanol, Hydrochlorid

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:71025-82-6 SDS

71025-82-6Downstream Products

71025-82-6Relevant academic research and scientific papers

Preparation of axially chiral biphenyl diphosphine ligands and their application in asymmetric hydrogenation

Morimoto, Toshiaki,Yoshikawa, Kiyoshi,Murata, Masanao,Yamamoto, Naoko,Achiwa, Kazuo

, p. 1445 - 1450 (2007/10/03)

Axially chiral biphenyldiphosphine ligands bearing diphenylphosphino group(s) and/or dicyclohexylphosphino group(s) were prepared in enantiomerically pure form starting from 2,6-dimethylnitrobenzene via 8 steps: iodination, reduction, methoxylation throug

Asymmetric Hydrogenation of α, β, and γ-Aminoketones Catalyzed by Cationic Rhodium(I){AMPP} Complexes

Devocelle, Marc,Agbossou, Francine,Mortreux, André

, p. 1306 - 1308 (2007/10/03)

The chiral cationic rhodium aminophosphine-phosphinite complexes 4-6 were applied successfully in the asymmetric hydrogenation of α- (7-9), β- (10, 11) and γ- (12) aminoketone hydrochloride derivatives leading to the corresponding aminoalcohols in up to 9

Efficient asymmetric hydrogenation of α-amino ketone derivatives. A highly enantioselective synthesis of phenylephrine, levamisole, carnitine and propranolol

Sukuraba,Takahashi,Takeda,Achiwa

, p. 738 - 747 (2007/10/02)

The complexes of pyrrolidine bisphosphine ligands (CPMs) with rhodium (I) were found to be efficient catalysts for asymmetric hydrogenation of α-amino ketone hydrochloride derivatives. Utilizing this methodology, we have developed efficient asymmetric syntheses of the optically active β-amino alcohols, phenylephrine, levamisole, carnitine and propranolol.

A new type of atropisomeric biphenylbisphosphine ligand, (R)-MOC-BIMPO and its use in efficient assymetric hydrogenation of α-aminoketone and itaconic acid

Yoshikawa,Yamamoto,Murata,Awano,Morimoto,Achiwa

, p. 13 - 16 (2007/10/02)

A new atropisomeric biphenylbisphosphine, MOC-BIMOP, has been prepared in enantiomerically pure form and its rhodium(I) complex proved to be an efficient catalyst in the asymmetric hydrogenations of α-aminoketone hydrochloride and itaconic acid. A possibl

Development of new 6-membered chelating chiral bisphosphine ligands for rhodium-catalyzed asymmetric hydrogenation

Inoguchi,Fujie,Yoshikawa,Achiwa

, p. 2921 - 2926 (2007/10/02)

A new chiral 1,3-bisphosphine, (1R,2R)-1-diphenylphosphino-2-(diphenylphosphinomethyl)cyclopentane, which was designed to form the favorable skew conformation of the six-membered chelate with rhodium, was developed. Its rhodium complex was found to be one of the most efficient catalysts known for asymmetric hydrogenation of amino acid precursors. Further improvement of this ligand was also attempted for catalytic asymmetric hydrogenation of prochiral ketones to clarify the enantioselective mechanism.

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