3005-62-7

Usage

Chemical Properties

White powder

InChI:InChI=1/C14H15N3O3/c1-20-14(19)12(7-11-8-15-9-16-11)17-13(18)10-5-3-2-4-6-10/h2-6,8-9,12H,7H2,1H3,(H,15,16)(H,17,18)

Upstream product

• 67-66-3 chloroform 
• 56-40-6 glycine 
• 4467-54-3 histidine methyl ester hydrochloride 
• 98-88-4 benzoyl chloride 
• 4467-54-3 l-histidine methyl ester dihydrochloride 
• 35166-50-8 1,N^α-dibenzoyl-histidine methyl ester 
• 72318-53-7 N^α-benzoyl-N^Im-tosyl-L-histidine methyl ester 
• 67-56-1 methanol 
• 5354-94-9 N-benzoyl-L-histidine 
• 65-85-0 benzoic acid 
• 1015244-09-3 (Z)-2-benzamido-4⁽⁵⁾-N-imidazolylpropenoic acid methyl ester 

Downstream Products

• 108839-11-8 1-acetyl-N^α-benzoyl-histidine-methyl ester 
• 102238-61-9 1-benzenesulfonyl-N^α-benzoyl-L-histidine-methyl ester 
• 97485-18-2 4-(1⁽³⁾H-imidazol-4-ylmethyl)-2-phenyl-4H-oxazol-5-one 
• 194797-41-6 N-[(S)-1-hydroxymethyl-2-(1⁽³⁾H-imidazol-4-yl)-ethyl]-benzamide 
• 24676-31-1 N^α-benzoyl-L-histidine amide 
• 95657-30-0 (S)-2-Benzoylamino-3-[3-((R)-2-hydroxy-propyl)-3H-imidazol-4-yl]-propionic acid methyl ester 
• 87867-17-2 N(α)-benzoyl-N(τ)-(2-acetoxyethyl)histidine methyl ester 
• 87867-16-1 N(α)-benzoyl-N(τ)-(2-benzyloxyethyl)histidine methyl ester 
• 95722-71-7 (S,αS)-N^α-benzoyl-N^τ-(2-hydroxypropyl)-L-histidine methyl ester 
• 95657-30-0 (S,αS)-N^α-benzoyl-N^?-(2-hydroxypropyl)-L-histidine methyl ester 
• 87867-09-2 N(α)-benzoyl-N(τ)-(2-hydroxy<2H5>propyl)histidine methyl ester 
• 145235-95-6 N(α)-benzoyl-N(τ)-(3-formyl-1-methoxymethylindol-2-yl)histidine methyl ester 
• 87867-18-3 N(α)-benzoyl-N(τ)-(2-benzyloxy<1,1,2,2-2H4>ethyl)histidine methyl ester 
• 72318-53-7 N^α-benzoyl-N^Im-tosyl-L-histidine methyl ester 

Relevant academic research and scientific papers

Functional ionic liquid mediated synthesis (FILMS) of dihydrothiophenes and tacrine derivatives

Natural amino acid-based functional ionic liquid [Bz-His(n-propyl) 2-OMe+Br-] promoted diastereoselective synthesis of dihydrothiophenes is described. Further this functional ionic liquid was efficiently utilized to form t

Theoretical evaluation on solubility of synthesized task specific ionic liquids in water

Task specific ionic liquids (TSILs) are synthesized and utilized for extraction of different metal atoms from their complexes. Since physico-chemical properties of ionic liquids (ILs) are modified by water (H2O) molecules, less hydrophilic ILs

Histidine and deuterium labelled histidine by asymmetric catalytic reduction with gaseous H2 or D2; the role of strong non-coordinating acids

An efficient and convenient route for the preparation of natural and unnatural histidine by asymmetric hydrogenation with rhodium-phosphine complexes is described. The reductions were performed in the presence of HBF4 to generate an essential imidazolyl cation. Stereoselective incorporation of D2 in the α,β-positions was obtained by catalytic deuteration in the presence of MeOD.

The Synthesis of N(τ)-(2-hydroxypropyl)histidine, N(τ)-2-hydroxyethyl)histidine, and Their Deuteriated Analogues

The synthesis of N(τ)-(2-hydroxypropyl)histidine (1), N(τ)-(2-hydroxypropyl)histidine (2), N(τ)-(2-hydroxyethyl)histidine (3), and N(τ)-(2-hydroxyethyl)histidine (4) by reaction of protected histidine derivatives with bromoacetone, bromoacetone, 2-benzyloxyethyl toluene-p-sulphonate (17), and 2-benzyloxyethyl toluene-p-sulphonate (18), respectively, is described.