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L-Phenylalanine, L-phenylalanylglycyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87742-85-6

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87742-85-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87742-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,4 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87742-85:
(7*8)+(6*7)+(5*7)+(4*4)+(3*2)+(2*8)+(1*5)=176
176 % 10 = 6
So 87742-85-6 is a valid CAS Registry Number.

87742-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[[2-[[(2S)-2-amino-3-phenylpropanoyl]amino]acetyl]amino]-3-phenylpropanoic acid

1.2 Other means of identification

Product number -
Other names L-Phenylalanine,L-phenylalanylglycyl

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:87742-85-6 SDS

87742-85-6Downstream Products

87742-85-6Relevant academic research and scientific papers

A genetically encodable ligand for transfer hydrogenation

Mayer, Clemens,Hilvert, Donald

supporting information, p. 3427 - 3431 (2013/07/19)

Simple tripeptides are shown here to be versatile ligands for iridium-catalyzed transfer hydrogenations affording large acceleration effects. A water-soluble iridium complex with Gly-Gly-Phe, for example, catalyzes the reduction of diverse ketones, aldehydes, and imines by formate with turnover frequencies rivaling or outperforming those of established ligand systems. Regioselective reduction of coenzyme NAD+ to NADH illustrates the potential utility of this system for biotechnological applications. Because peptides are genetically encodable, they represent an attractive class of foldamer ligands for creating artificial metalloenzymes.

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