4582-71-2

Basic information

• Product Name: N-benzoylserine
• Synonyms: 2-(benzoylamino)-3-hydroxypropanoic acid; benzoylserine
• CAS NO: 4582-71-2
• Molecular Formula: C₁₀H₁₁NO₄
• Molecular Weight: 209.1986
• Mol File: 4582-71-2.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 528.5°C at 760 mmHg
• Flash Point: 273.4°C
• Density: 1.347g/cm³
• Vapor Pressure: 5.33E-12mmHg at 25°C
• Refractive Index: 1.587
• CAS DataBase Reference: N-benzoylserine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzoylserine(4582-71-2)
• EPA Substance Registry System: N-benzoylserine(4582-71-2)

Safety Data

• Hazardous Substances Data: 4582-71-2(Hazardous Substances Data)

Usage

General Description

N-benzoylserine is a compound that belongs to the family of organic compounds known as benzoic acids and derivatives. It is derived from the naturally occurring amino acid serine, which is a building block for proteins in the body. N-benzoylserine has a benzoyl group attached to the amino group of serine, making it a derivative of the amino acid. N-benzoylserine has been studied for its potential pharmaceutical and biological applications, especially in the field of drug design and development. It exhibits certain biological activities, and its structure allows for modifications to be made in order to improve its pharmacological properties. Researchers are interested in exploring the therapeutic potential of N-benzoylserine in the treatment of various diseases and conditions.

Upstream product

• 56-23-5 tetrachloromethane 
• 1504-19-4 N-benzoyl-O-benzyl-DL-serine 
• 302-84-1 serin 
• 98-88-4 benzoyl chloride 
• 58156-44-8 2,4,6-trinitrophenyl benzoate 
• 56-45-1 L-serin 
• 1102900-87-7 N-(p-methylbenzoyl)-L-serine 
• 80548-05-6 2-benzoylamino-3-oxo-propionic acid ethyl ester 
• 83044-84-2 O-benzoyl-DL-serine 
• 4783-22-6 N-benzoyl-serine ethyl ester 

Downstream Products

• 99184-99-3 (R)-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid 
• 1040384-28-8 N-benzoyl-D-serine methyl ester 
• 21611-54-1 N-benzoyl-3-chloro-alanine ethyl ester 
• 112575-28-7 (Z)-2-Benzoylamino-3-bromo-acrylic acid 4-nitro-benzyl ester 
• 112575-28-7 N-benzoyl-3-bromodehydroalanine p-nitrobenzyl ester 
• 112575-27-6 N-benzoyldehydroalanine p-nitrobenzyl ester 
• 112575-29-8 N-benzoyl-3-bromodehydroalanine 
• 112575-25-4 2-phenyl-4-(bromomethylidene)-5(4H)-oxazolone 
• 112575-26-5 N-benzoyl-DL-serine p-nitrobenzyl ester 
• 124613-28-1 2-(benzylamino)propane-1,3-diol 
• 20989-42-8 N-benzoylserine methyl ester 
• 86808-09-5 N-(p-methylbenzoyl)-D-serine 
• 4877-23-0 (S)-2-benzoylamino-3-hydroxypropionic acid 
• 4783-22-6 N-benzoyl-serine ethyl ester 

Relevant articles and documents

Reactivity of Tyrosyl–Proline toward Benzoylation in Aqueous 1,4-Dioxane

Abstract: The kinetics of the reaction of L-tyrosyl-L-proline (Tyr–Pro) with di- andtrinitrophenyl benzoates in aqueous 1,4-dioxane (40 wt percent of water) were studiedin the temperature range 298–313 K. The reaction rate constant k298 was fou

Skin care

PROBLEM TO BE SOLVED: To provide a skin care preparation suitable for a cosmetic (including quasi medicine). SOLUTION: The skin care preparation comprises a compound represented by general formula (1) [wherein R1is a hydrogen ato

Reactivity of the Amino Groups of α-Amino Acids and Dipeptides in Reaction with Benzoyl Chloride in a Dioxane-Water Solvent

The kinetic characteristics (rate constants, activation energies, and entropies of activation) for the reaction of a series of α-amino acids and dipeptides with benzoyl chloride in aqueous dioxane are presented.The amino group in the investigated α-amino acids has high reactivity 4 liter/mole*sec>; the dipeptides have lower reactivity 3 liter/mole*sec>.