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153322-11-3

(1R,2S)-N-BENZYL-2-AMINO-1,2-DIPHENYLETHANOL is a chiral compound belonging to the class of amino alcohols. It is a synthetic compound characterized by the presence of a benzyl group, an amino group, and a diphenylethanol moiety in its structure. (1R,2S)-N-BENZYL-2-AMINO-1,2-DIPHENYLETHANOL is utilized in organic chemistry as a chiral auxiliary for the asymmetric synthesis of various organic molecules. Its unique structural features also make it a valuable molecule for medicinal chemistry research and drug discovery, with potential pharmacological or biological activities.

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  • 153322-11-3 Structure

  • Basic information

    1. Product Name: (1R,2S)-N-BENZYL-2-AMINO-1,2-DIPHENYLETHANOL
    2. Synonyms: Benzeneethanol, .alpha.-phenyl-.beta.-[(phenylmethyl)amino]-, (.alpha.R,.beta.S)-
    3. CAS NO:153322-11-3
    4. Molecular Formula: C21H21NO
    5. Molecular Weight: 303.405
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153322-11-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 465.9°C at 760 mmHg
    3. Flash Point: 122.2°C
    4. Appearance: /
    5. Density: 1.132g/cm3
    6. Vapor Pressure: 1.76E-09mmHg at 25°C
    7. Refractive Index: 1.623
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: (1R,2S)-N-BENZYL-2-AMINO-1,2-DIPHENYLETHANOL(CAS DataBase Reference)
    11. NIST Chemistry Reference: (1R,2S)-N-BENZYL-2-AMINO-1,2-DIPHENYLETHANOL(153322-11-3)
    12. EPA Substance Registry System: (1R,2S)-N-BENZYL-2-AMINO-1,2-DIPHENYLETHANOL(153322-11-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 153322-11-3(Hazardous Substances Data)

153322-11-3 Usage

Uses

Used in Organic Chemistry:
(1R,2S)-N-BENZYL-2-AMINO-1,2-DIPHENYLETHANOL is used as a chiral auxiliary for the asymmetric synthesis of various organic molecules. Its unique structure allows for the creation of enantiomerically pure compounds, which is crucial in the development of pharmaceuticals and other specialty chemicals.
Used in Medicinal Chemistry Research:
(1R,2S)-N-BENZYL-2-AMINO-1,2-DIPHENYLETHANOL is used as a valuable molecule in medicinal chemistry research. Its structural features make it a promising candidate for the development of new drugs, as it can be modified and optimized for specific biological targets.
Used in Drug Discovery:
(1R,2S)-N-BENZYL-2-AMINO-1,2-DIPHENYLETHANOL is used in drug discovery for its potential pharmacological or biological activities. Its unique structure and chiral properties make it a versatile starting point for the design and synthesis of novel therapeutic agents.
Used in Pharmaceutical Industry:
(1R,2S)-N-BENZYL-2-AMINO-1,2-DIPHENYLETHANOL is used as a key intermediate in the synthesis of pharmaceutical compounds. Its ability to influence the stereochemistry of target molecules makes it an essential component in the development of enantiomerically pure drugs, which can have significant implications for the safety and efficacy of medications.

Check Digit Verification of cas no

The CAS Registry Mumber 153322-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,3,2 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 153322-11:
(8*1)+(7*5)+(6*3)+(5*3)+(4*2)+(3*2)+(2*1)+(1*1)=93
93 % 10 = 3
So 153322-11-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H21NO/c23-21(19-14-8-3-9-15-19)20(18-12-6-2-7-13-18)22-16-17-10-4-1-5-11-17/h1-15,20-23H,16H2/t20-,21+/m0/s1

153322-11-3SDS

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 (1R,2S)-2-(benzylamino)-1,2-diphenylethanol

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:153322-11-3 SDS

153322-11-3Relevant articles and documents

Evolution of chiral Lewis basic N-formamide as highly effective organocatalyst for asymmetric reduction of both ketones and ketimines with an unprecedented substrate scope

Zhou, Li,Wang, Zhouyu,Wei, Siyu,Sun, Jian

, p. 2977 - 2979 (2008/02/12)

L-Pipecolinic acid derived Lewis basic N-formamide 5e has been developed as a first highly effective catalyst for the asymmetric reduction of aromatic and aliphatic ketones as well as aromatic and aliphatic ketimines in good to high enantioselectivity. The Royal Society of Chemistry.

Easily accessible chiral amino-phosphinite ligands for highly enantioselective palladium-mediated allylic alkylation

Chen, Guoshu,Li, Xin,Zhang, Haile,Gong, Liuzhu,Mi, Aiqiao,Cui, Xin,Jiang, Yaozhong,Choi, Michael C.K.,Chan, Albert S.C.

, p. 809 - 813 (2007/10/03)

Palladium-catalyzed asymmetric allylic alkylation of 1,3-diphenyl-2-propenyl acetate with the dimethyl malonate-BSA-LiOAc system has been successfully carried out in the presence of easily prepared new chiral amino-phosphinite ligands such as 3b and 3c to

Amino alcohol coordination in ruthenium(II)-catalysed asymmetric transfer hydrogenation of ketones

Petra, Danielle G. I.,Kamer, Paul C. J.,Van Leeuwen, Piet W. N. M.,Goubitz, Kees,Van Loon, Arjen M.,De Vries, Johannes G.,Schoemaker, Hans E.

, p. 2335 - 2341 (2007/10/03)

The nature of ruthenium-amino alcohol precursors in the catalytic cycle of asymmetric hydrogen transfer reactions was studied using two C2- symmetrical tetradentate ligands (1 and 2) that were synthesised from (nor)ephedrine. The structure of t

ONE POT SYNTHESIS OF HOMOCHIRAL AZIRIDINES AND AMINOALCOHOLS FROM HOMOCHIRAL 1,2-CYCLIC SULFATES

Lohray, B. Bhushan,Gao, Yun,Sharpless, K. Barry

, p. 2623 - 2626 (2007/10/02)

Preparations of homochiral N-substituted aziridines and aminoalcohols from 1,2-cyclic sulfates are reported.Primary amines react with cyclic sulfates to give β-aminosulfates which can be converted either to aziridines or to aminoalcohols by treatment with

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