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138165-77-2

138165-77-2

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138165-77-2 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 138165-77-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,6 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 138165-77:
(8*1)+(7*3)+(6*8)+(5*1)+(4*6)+(3*5)+(2*7)+(1*7)=142
142 % 10 = 2
So 138165-77-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2.ClH/c11-9(7-10(12)13)6-8-4-2-1-3-5-8;/h1-5,9H,6-7,11H2,(H,12,13);1H/t9-;/m1./s1

138165-77-2 Well-known Company Product Price

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  • Sigma-Aldrich

  • (03769)  L-β-Homophenylalaninehydrochloride  ≥98.0%

  • 138165-77-2

  • 03769-250MG

  • 2,311.92CNY

  • Detail

138165-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name L-Beta-Homophenylalanine Hydrochloride

1.2 Other means of identification

Product number -
Other names (3S)-3-amino-4-phenylbutanoic acid,hydrochloride

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:138165-77-2 SDS

138165-77-2Relevant articles and documents

Improved enzymatic syntheses of valuable β-arylalkyl-β-amino acid enantiomers

Tasnadi, Gabor,Forro, Enik,Fueloep, Ferenc

experimental part, p. 793 - 799 (2010/06/20)

The enantioselective (E～ 200) Burkholderia cepacia-catalysed hydrolyses of β-amino esters with H2O (0.5 equiv.) in t-BuOMe or in i-Pr2O at 45 °C are described. The enantiomers of biologically relevant β-arylalkyl-substituted β-amino acids, and especially (R)-3-amino-3-(2,4,5-trifluorophenyl)butanoic acid, the intermediate of the new antidiabetic drug sitagliptine, were prepared with high enantiomeric excesses (ee≥96%) and in good yields (≥42%). The Royal Society of Chemistry 2010.

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