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167479-78-9

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167479-78-9 Usage

Uses

4-Cyano-L-phenylalanine used as a intermediate in organic synthesis, pharmaceutical, chemical research and biochemical application.

Check Digit Verification of cas no

The CAS Registry Mumber 167479-78-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,4,7 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 167479-78:
(8*1)+(7*6)+(6*7)+(5*4)+(4*7)+(3*9)+(2*7)+(1*8)=189
189 % 10 = 9
So 167479-78-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O2/c11-6-8-3-1-7(2-4-8)5-9(12)10(13)14/h1-4,9H,5,12H2,(H,13,14)/t9-/m0/s1

167479-78-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H63572)  4-Cyano-L-phenylalanine, 98%   

  • 167479-78-9

  • 250mg

  • 375.0CNY

  • Detail
  • Alfa Aesar

  • (H63572)  4-Cyano-L-phenylalanine, 98%   

  • 167479-78-9

  • 1g

  • 1000.0CNY

  • Detail
  • Alfa Aesar

  • (H63572)  4-Cyano-L-phenylalanine, 98%   

  • 167479-78-9

  • 5g

  • 3753.0CNY

  • Detail

167479-78-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-Amino-3-(4-cyanophenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names L-4-Cyanophenylalanine

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:167479-78-9 SDS

167479-78-9Relevant articles and documents

The bacterial ammonia lyase EncP: A tunable biocatalyst for the synthesis of unnatural amino acids

Weise, Nicholas J.,Parmeggiani, Fabio,Ahmed, Syed T.,Turner, Nicholas J.

supporting information, p. 12977 - 12983 (2015/10/28)

Enzymes of the class I lyase-like family catalyze the asymmetric addition of ammonia to arylacrylates, yielding high value amino acids as products. Recent examples include the use of phenylalanine ammonia lyases (PALs), either alone or as a gateway to deracemization cascades (giving (S)- or (R)-α-phenylalanine derivatives, respectively), and also eukaryotic phenylalanine aminomutases (PAMs) for the synthesis of the (R)-β-products. Herein, we present the investigation of another family member, EncP from Streptomyces maritimus, thereby expanding the biocatalytic toolbox and enabling the production of the missing (S)-β-isomer. EncP was found to convert a range of arylacrylates to a mixture of (S)-α- and (S)-β-arylalanines, with regioselectivity correlating to the strength of electron-withdrawing/-donating groups on the ring of each substrate. The low regioselectivity of the wild-type enzyme was addressed via structure-based rational design to generate three variants with altered preference for either α- or β-products. By examining various biocatalyst/substrate combinations, it was demonstrated that the amination pattern of the reaction could be tuned to achieve selectivities between 99:1 and 1:99 for β:α-product ratios as desired.

Fluorobenzamidrazone thrombin inhibitors: Influence of fluorine on enhancing oral absorption

Lee, Koo,Jung, Won-Hyuk,Sang, Yeul Hwang,Lee, Sung-Hack

, p. 2483 - 2486 (2007/10/03)

LB30057 (1) is a selective and efficacious oral thrombin inhibitor. Fluorine-substitution on the phenylene ring of the benzamidrazone portion in both compound 1 and its derivatives gave, in many cases, enhanced oral absorption in rats while maintaining the intrinsic potency and selectivity. Compound 2 demonstrated a 3-fold increase in absorption.

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