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83509-88-0

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83509-88-0 Usage

General Description

Z--HOMOALA-OH is a chemical compound that belongs to the class of organic compounds known as alpha-hydroxy ketones. It is a rare chemical compound and its properties and uses are not widely documented. However, based on its structure, it is likely to have applications in organic synthesis, as well as in the pharmaceutical and chemical industries. It contains a ketone group and a hydroxyl group, which make it a potential intermediate in the synthesis of various organic compounds. Its specific uses and properties would need to be further explored and researched.

Check Digit Verification of cas no

The CAS Registry Mumber 83509-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,0 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83509-88:
(7*8)+(6*3)+(5*5)+(4*0)+(3*9)+(2*8)+(1*8)=150
150 % 10 = 0
So 83509-88-0 is a valid CAS Registry Number.

83509-88-0 Well-known Company Product Price

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  • Aldrich

  • (61669)  Z-β-Homoala-OH  ≥98.0% (HPLC)

  • 83509-88-0

  • 61669-500MG-F

  • 4,014.27CNY

  • Detail

83509-88-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-3-(phenylmethoxycarbonylamino)butanoic acid

1.2 Other means of identification

Product number -
Other names (3S)-benzyloxycarbonylaminobutyric acid

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:83509-88-0 SDS

83509-88-0Relevant articles and documents

Synthesis of enantiopure free and N-benzyloxycarbonyl-protected 3-substituted homotaurines from naturally occurring amino acids

Zheng, Yongpeng,Xu, Jiaxi

, p. 5197 - 5206 (2014/07/08)

Enantiopure N-benzyloxycarbonyl-protected and free 3-substituted homotaurines were synthesized from naturally occurring amino acids via N-benzyloxycarbonyl protection, Arndt-Eistert homologation, reduction, esterification with thioacetic acid, and oxidation with performic acid. The current method is a convenient, practical, and salt-free method for the synthesis of enantiopure 3-substituted homotaurine with moderate to good yields.

Synthesis of enantiopure free and N-benzyloxycarbonyl-protected 3-substituted homotaurines from naturally occurring amino acids

Zheng, Yongpeng,Xu, Jiaxi

, p. 5197 - 5206 (2014/12/10)

Enantiopure N-benzyloxycarbonyl-protected and free 3-substituted homotaurines were synthesized from naturally occurring amino acids via N-benzyloxycarbonyl protection, Arndt-Eistert homologation, reduction, esterification with thioacetic acid, and oxidation with performic acid. The current method is a convenient, practical, and salt-free method for the synthesis of enantiopure 3-substituted homotaurine with moderate to good yields.

Synthesis of novel N-protected β3-amino nitriles: study of their hydrolysis involving a nitrilase-catalyzed step

Veitia, Maite Sylla-Iyarreta,Brun, Pierre Louis,Jorda, Pierre,Falguieres, Annie,Ferroud, Clotilde

experimental part, p. 2077 - 2089 (2010/03/04)

Several commercially available nitrilases were investigated with regard to their potential to hydrolyze N-protected β3-amino nitriles into their corresponding N-protected β3-amino acids. The biotransformations were obtained in different proportions depending on the nitrilase involved. The best hydrolysis results were achieved for the N-Cbz-β3-amino nitrile from l-alanine using the NIT-107, in a phosphate buffer at 0.05 M. However, no biotransformation into the corresponding acids was observed for the N-sulfonylamide β3-amino nitriles. Two simple and efficient procedures to prepare the β3-amino nitriles from their analogous α-amino acids are described. Thirty four new substances were synthesized and characterized over the course of this work.

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