31534-22-2

Basic information

• Product Name: poly(1-benzylhistidine)
• Synonyms: poly(1-benzylhistidine)
• CAS NO: 31534-22-2
• Molecular Formula: C13H15N3O2
• Molecular Weight: 245.2771
• Mol File: 31534-22-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 484.8°Cat760mmHg
• Flash Point: 247°C
• Appearance: /
• Density: 1.27g/cm³
• Vapor Pressure: 3.29E-10mmHg at 25°C
• Refractive Index: 1.627
• CAS DataBase Reference: poly(1-benzylhistidine)(CAS DataBase Reference)
• NIST Chemistry Reference: poly(1-benzylhistidine)(31534-22-2)
• EPA Substance Registry System: poly(1-benzylhistidine)(31534-22-2)

Safety Data

• Hazardous Substances Data: 31534-22-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H15N3O2/c14-12(13(17)18)6-11-8-16(9-15-11)7-10-4-2-1-3-5-10/h1-5,8-9,12H,6-7,14H2,(H,17,18)/t12-/m0/s1

Upstream product

• 100-44-7 benzyl chloride 
• 71-00-1 L-histidine 
• 71-00-1 L-histidine 
• 20898-44-6 Boc-His(Bzl)-OH 

Downstream Products

• 65717-64-8 N-(t-butoxycarbonyl)-^im-benzyl-D-histidine 
• 122766-72-7 1-benzyl-N^α-(1-benzyl-N^α-benzyloxycarbonyl-L-histidyl)-L-histidine-benzyl ester 
• 122411-85-2 1benzyl-N^α-(N-benzyloxycarbonyl-L-phenylalanyl)-L-histidine-hydrazide 
• 120548-57-4 N-(1-benzyl-N^α-benzyloxycarbonyl-L-histidyl)-glycine-benzyl ester 
• 105374-43-4 N-(1-benzyl-N^α-benzyloxycarbonyl-L-histidyl)-glycine 
• 104882-34-0 1-benzyl-N^α-methyl-N^α-(toluene-4-sulfonyl)-L-histidine 
• 459157-89-2 N_im-benzyl-spinacine methyl ester 
• 93983-56-3 τ-benzyl-L-histidine methyl ester dihydrochloride 
• 768322-42-5 N_im-benzyl-spinacine 
• 127064-07-7 1-benzyl-4-<2'-(acetylamino)-3'-hydroxypropyl>imidazole 
• 909278-46-2 1-benzyl-N^α-(toluene-4-sulfonyl)-L-histidine 
• 21929-66-8 N^α-carbobenzoxy-N^im-benzyl-L-histidine 
• 96216-64-7 1-benzyl-N^α-[4-(4-methoxy-phenylazo)-benzyloxycarbonyl]-histidine 

Relevant articles and documents

PROCESS FOR SYNTHESIZING ERGOTHIONEINE AND RELATED COMPOUNDS

The invention provides a process for synthesising a compound of formula (V) wherein: formula (z) or a physiologically acceptable salt, tautomer, stereoisomer or mixture of stereoisomers thereof. The process utilizes a /V-benzyl protected histidine rather

Regiospecific alkylation of histidine and histamine at N-1 (τ)

Series of 1-alkyl histidines and histamines have been synthesized by the alkylation of the corresponding 5,6,7,8-tetrahydro-5-oxomidazo[1,5-c]pyrimidines with alkyl halides in aprotic solvents. The method of conversion of the intermediate quaternary salt to the amino acid or amino depends on the nature of the alkyl group.

CYCLIC CARBAMATE ANALOGUES OF (+)-PILOCARPINE

Pilocarpine analogues are provided having the structure STR1 where one of R 1 or R 2 is an alkyl, such as methyl, ethyl, propyl, butyl, and so forth, and the corresponding secondary alkyl groups, an aralkyl, such as benzyl, phenylethyl, phenylpropyl, and the corresponding secondary aralkyl residues, or a cycloalkyl having less than about 12 carbon atoms. R 3 has at least two carbon atoms but less than about 9. These pilocarpine analogues have improved duration of biological activity with respect to pilocarpine. A particularly preferred compound is a muscarinic agonist equipotent with pilocarpine, where R 2 is methyl, and R 3 is ethyl.