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6331-09-5

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  • China Largest factory Manufacturer Supply D-ALANINE ETHYL ESTER HYDROCHLORIDE CAS 6331-09-5

    Cas No: 6331-09-5

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6331-09-5 Usage

Uses

D-Alanine ethyl ester hydrochloride is used as organic intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 6331-09-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6331-09:
(6*6)+(5*3)+(4*3)+(3*1)+(2*0)+(1*9)=75
75 % 10 = 5
So 6331-09-5 is a valid CAS Registry Number.

6331-09-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H62791)  D-Alanine ethyl ester hydrochloride, 95%   

  • 6331-09-5

  • 5g

  • 341.0CNY

  • Detail
  • Alfa Aesar

  • (H62791)  D-Alanine ethyl ester hydrochloride, 95%   

  • 6331-09-5

  • 25g

  • 1362.0CNY

  • Detail

6331-09-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (2R)-2-aminopropanoate,hydrochloride

1.2 Other means of identification

Product number -
Other names (R)-Alanine ethyl ester 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:6331-09-5 SDS

6331-09-5Relevant articles and documents

Silver ion-induced chiral enhancement by argentivorous molecules

Lee, Eunji,Hosoi, Yasuhiro,Temma, Honoka,Ju, Huiyeong,Ikeda, Mari,Kuwahara, Shunsuke,Habata, Yoichi

supporting information, p. 3373 - 3376 (2020/03/31)

Optically active tetra-armed cyclens with an asymmetric chiral centre in the cyclen moiety were synthesized and were shown to enhance chirality and control of enantiomers on complexation with Ag+. Binding studies of the Ag+ complex demonstrated that Ag+ preferentially interacts with electron-rich substituents over other aromatic substituents.

AN EFFICIENT SYNTHESIS OF N-HYDROXY-α-AMINO ACID DERIVATIVES OF HIGH OPTICAL PURITY.

Feenstra, R. W.,Stokkingreef, E. H. M.,Nivard, R. J. F.,Ottenheijm, H. C. J.

, p. 1215 - 1218 (2007/10/02)

Conversion of α-hydroxy esters via triflates into compounds 3 proceeds in chemical yields ranging from 78 to 89percent and with optical purities ranging from 76 to 100percent.

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