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58780-66-8

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58780-66-8 Usage

General Description

Phenylalanine, phenylmethyl ester hydrochloride (1:1) is a chemical compound that consists of a 1:1 ratio of phenylalanine and phenylmethyl ester, with the addition of hydrochloride. Phenylalanine is an essential amino acid that is important for the synthesis of proteins and the production of neurotransmitters such as dopamine and norepinephrine. Phenylmethyl ester is an ester form of phenylalanine that is commonly used in the synthesis of pharmaceuticals and as a flavoring agent. The addition of hydrochloride increases the solubility of the compound in water. This chemical compound has potential applications in the pharmaceutical and food industries.

Check Digit Verification of cas no

The CAS Registry Mumber 58780-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,8 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58780-66:
(7*5)+(6*8)+(5*7)+(4*8)+(3*0)+(2*6)+(1*6)=168
168 % 10 = 8
So 58780-66-8 is a valid CAS Registry Number.

58780-66-8SDS

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 benzyl 2-amino-3-phenylpropanoate

1.2 Other means of identification

Product number -
Other names Phenylalanine O-benzyl 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:58780-66-8 SDS

58780-66-8Relevant articles and documents

Unusual reactivity of nitronates with an aryl alkyl carbonate: Synthesis of α-amino esters

Reddy, Golipalli Ramana,Mukherjee, Debopreeti,Chittoory, Arjun Kumar,Rajaram, Sridhar

, p. 5874 - 5877 (2015/01/08)

The monoanions of nitroalkanes are ambident nucleophiles that react with carbonate electrophiles through the oxygen atom. Products arising from reactivity at the carbon atom will yield α-nitro esters, which are precursors for α-amino esters. We demonstrate this in the reactions of nitroalkanes with benzyl phenyl carbonate and DABCO where α-nitro esters are obtained instead of nitrile oxides. The products are readily reduced to α-amino esters. This pathway could be a safe alternative to the Strecker reaction.

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