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500770-82-1

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500770-82-1 Usage

General Description

(S)-BOC-4-CYANO-BETA-PHE-OH is a chemical compound with the molecular formula C16H19NO4. It is a derivative of beta-phenylalanine, which is an amino acid. The compound contains a BOC (tert-butyloxycarbonyl) protective group, which is commonly used in organic synthesis to protect amines. The presence of a cyano group (CN) makes this compound a nitrile derivative. This chemical may be used in the synthesis of various pharmaceuticals and organic compounds, and its properties make it useful in peptide synthesis and other organic chemistry applications.

Check Digit Verification of cas no

The CAS Registry Mumber 500770-82-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,7,7 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 500770-82:
(8*5)+(7*0)+(6*0)+(5*7)+(4*7)+(3*0)+(2*8)+(1*2)=121
121 % 10 = 1
So 500770-82-1 is a valid CAS Registry Number.

500770-82-1 Well-known Company Product Price

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  • Aldrich

  • (44376)  (S)-Boc-4-cyano-β-Phe-OH  ≥98.0%

  • 500770-82-1

  • 44376-500MG-F

  • 3,535.74CNY

  • Detail

500770-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-3-(4-cyanophenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

1.2 Other means of identification

Product number -
Other names Boc-4-cyano-D-|A-phenylalanine

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:500770-82-1 SDS

500770-82-1Relevant articles and documents

Synthesis of the enantiomers and N-protected derivatives of 3-amino-3-(4-cyanophenyl)propanoic acid

Solymar, Magdolna,Kanerva, Liisa T.,Fueloep, Ferenc

, p. 1893 - 1897 (2007/10/03)

Racemic ethyl 3-amino-3-(4-cyanophenyl)propanoate was synthesized and the enantiomers separated through enantioselective N-acylation by Candida antarctica lipase A (CAL-A) in neat butyl butanoate. The free amino acid enantiomers were transformed to the Boc and Fmoc-protected derivatives.

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