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L-Phenylalanine, N-[3-(2-furanyl)-1-oxo-2-propenyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65376-39-8

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65376-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65376-39-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,7 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65376-39:
(7*6)+(6*5)+(5*3)+(4*7)+(3*6)+(2*3)+(1*9)=148
148 % 10 = 8
So 65376-39-8 is a valid CAS Registry Number.

65376-39-8SDS

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 N-[3-(2-furyl)acryloyl]-phenylalanine methyl ester

1.2 Other means of identification

Product number -
Other names N-furylacryloylphenylalanine methyl ester

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:65376-39-8 SDS

65376-39-8Downstream Products

65376-39-8Relevant academic research and scientific papers

Synthesis of some amino acid and peptide conjugates and their evaluation as potential anti-allergic and anti-inflammatory agents

Shalaby,Abd Al-Salam,Kalmouch,El-Shihaby,Abdullah

, p. 401 - 415 (2015/10/20)

ANEW series of N-3-(2-furanyl) acryloyl, N-3-(5-methyl)-2-(furanyl)-acryoyl amino acids, peptide and piprazines amids, were structurally designed and synthesized. About 23 compounds (5a-w) were synthesized and their anti-allergic and anti-inflamatory acti

Carboxamidation of carboxylic acids with 1-tert-butoxy-2-tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI) without bases

Saito, Yukako,Ouchi, Hidekazu,Takahata, Hiroki

experimental part, p. 11129 - 11135 (2009/04/11)

Formation of carboxamides of a variety of carboxylic acids with the coupling reagent BBDI is described. This procedure permits a one pot and simple operation without the need of any bases and no base was?required for even use of amine hydrochlorides. In addition, an approach to BBDI-catalyzed carboxamidation is examined.

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