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L-Phenylalanine, N-acetyl-4-(chloromethyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130887-73-9

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130887-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130887-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,8,8 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130887-73:
(8*1)+(7*3)+(6*0)+(5*8)+(4*8)+(3*7)+(2*7)+(1*3)=139
139 % 10 = 9
So 130887-73-9 is a valid CAS Registry Number.

130887-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ac-L-Phe(4-CH2Cl)-OEt

1.2 Other means of identification

Product number -
Other names N-Ac-L-Phe(p-CH2Cl).OEt

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:130887-73-9 SDS

130887-73-9Relevant academic research and scientific papers

Synthesis of Human CCK26-33 and CCK-33 Related Analogues on 2,4-DMBHA and TMBHA

Miranda, Maria Teresa Machini,Liddle, Rodger A.,Rivier, Jean E.

, p. 1681 - 1688 (1993)

New analogues of human cholecystokinin in which the Tyr(SO3H) has been replaced by Phe(p-CH2SO3Na), methionines by norleucines, and tryptophan by 2-naphthylalanine27,Nle28,31,Nal30>-CCK26-33 and

An efficient synthesis of N(α)-FMOC-4(phosphonomethyl)-L- and D- phenylalanine

Bo, Liu,Jiarong, Zhan

, p. 2293 - 2299 (2007/10/03)

A simple and efficient synthesis for N(α)-Fmoc-4-(phosphonomethyl)L- phenylalanine and N(α)-Fmoc-D-phenylalanine with high optical purity by using the commercially available L and D-phenylalanine as the starting material is described.

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