58780-66-8 Usage
Uses
Used in Pharmaceutical Industry:
Phenylalanine, phenylmethyl ester, hydrochloride (1:1) is used as an intermediate in the synthesis of various pharmaceuticals for its role in the production of essential amino acids and neurotransmitters.
Used in Food Industry:
Phenylalanine, phenylmethyl ester, hydrochloride (1:1) is used as a flavoring agent to enhance the taste and aroma of food products, taking advantage of its ester form's properties in creating desirable flavors.
Used in Research and Development:
Phenylalanine, phenylmethyl ester, hydrochloride (1:1) serves as a valuable compound in scientific research for studying the properties and functions of amino acids and their derivatives, as well as their potential applications in medicine and other fields.
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.
58780-66-8Relevant academic research and scientific papers
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.
Esterification process
-
, (2008/06/13)
Esters are formed by reacting an amino carboxylic acid with an alkylating agent in an aprotic solvent.
