5910-52-1

Basic information

• Product Name: 1-methyl N-L-alpha-aspartyl-3-phenyl-L-alaninate monohydrochloride
• Synonyms: 1-methyl N-L-alpha-aspartyl-3-phenyl-L-alaninate monohydrochloride
• CAS NO: 5910-52-1
• Molecular Formula: C₁₄H₁₈N₂O₅*ClH
• Molecular Weight: 330.76406
• EINECS: 227-623-2
• Mol File: 5910-52-1.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-methyl N-L-alpha-aspartyl-3-phenyl-L-alaninate monohydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl N-L-alpha-aspartyl-3-phenyl-L-alaninate monohydrochloride(5910-52-1)
• EPA Substance Registry System: 1-methyl N-L-alpha-aspartyl-3-phenyl-L-alaninate monohydrochloride(5910-52-1)

Safety Data

• Hazardous Substances Data: 5910-52-1(Hazardous Substances Data)

Usage

Explanation

Different sources of media describe the Explanation of 5910-52-1 differently. You can refer to the following data:
1. This is the chemical name of the compound, which is a dipeptide derivative.
2. The compound has potential uses in the pharmaceutical industry due to its possible therapeutic effects.
3. It is derived from two amino acids and has potential therapeutic properties.
4. The compound may help reduce inflammation and relieve pain in the body.
5. Studies have been conducted on the compound for its potential use in managing long-term pain and inflammation.
6. The monohydrochloride form of the compound makes it suitable for pharmaceutical applications.
7. Further research and development of this compound may lead to the creation of new medications for a range of health issues.

Industry

Pharmaceutical

Classification

Dipeptide derivative

Potential effects

Anti-inflammatory and analgesic

Applications

Treatment of chronic pain and inflammatory conditions

Form

Monohydrochloride

Future development

New drugs for various medical conditions

Upstream product

• 41567-23-1 anhydride du N-chloroacetyl-L-acide aspartique 
• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 
• 63-91-2 L-phenylalanine 
• 4976-94-7 Boc-Asp(OtBu)-Phe-OMe 
• 33605-76-4 N-formylaspartame 
• 22839-82-3 N-α-L-aspartyl-L-phenylalaninemethyl ester 
• 67-56-1 methanol 

Downstream Products

• 22839-47-0 L-Asp-L-Phe-OMe 

Relevant articles and documents

METHOD FOR THE SYNTHESIS OF PEPTIDES WITHOUT SOLVENT

The disclosure relates to a method for the synthesis of a compound of the formula (I) in which: n is an integer higher than or equal to 1; Rb and each Rn are independently a hydrogen atom, a C1-C6 arylalkyl group or a C1-C6 alkyl group substituted or not by an aryl group, —COOH, C1-C6, —COO-(alkyl), —CONH2, —SH, heteroaryl, —NH2, —NHC(NH)(NH2), C1-C6-s-(alkyl), —OH or phenol; Ra is a N-protective group; Rc is a ORd group in which Rd is a C1-C6 alkyl group or a NReRf group in which Re and Rf Re independently an N-protective group.

Process for the preparation of alfa-L-aspartyl-L-phenyl-alanine alkyl esters

A new process for preparing alfa-L-aspartyl-L-phenylalanine alkyl esters of formula I STR1 wherein R represents an alkyl group having from 1 to 5 carbon atoms, starting from the corresponding alfa-haloacyl-alfa-L-aspartyl-L-phenylalanine alkyl esters.

An N-Carboxyanhydride (NCA) Route to Aspartame

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