15742-88-8

Basic information

• Product Name: 4-hydroxymethylphenylalanine
• Synonyms: 4-hydroxymethylphenylalanine;L-4-hydroxymethyl-Phenylalanine
• CAS NO: 15742-88-8
• Molecular Formula: C₁₀H₁₃NO₃
• Molecular Weight: 195.22
• Mol File: 15742-88-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 397°Cat760mmHg
• Flash Point: 193.9°C
• Appearance: /
• Density: 1.29g/cm³
• Vapor Pressure: 5.14E-07mmHg at 25°C
• Refractive Index: 1.602
• CAS DataBase Reference: 4-hydroxymethylphenylalanine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxymethylphenylalanine(15742-88-8)
• EPA Substance Registry System: 4-hydroxymethylphenylalanine(15742-88-8)

Safety Data

• Hazardous Substances Data: 15742-88-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H13NO3/c11-9(10(13)14)5-7-1-3-8(6-12)4-2-7/h1-4,9,12H,5-6,11H2,(H,13,14)

Upstream product

• 160916-46-1 N-boc-4-hydroxymethylphenylalanine 
• 216774-50-4 N-tert-butyloxycarbonyl-(p-hydroxymethyl)-L-phenylalanine methyl ester 
• 216774-45-7 methyl 2-(S)-((tert-butoxycarbonyl)amino)-3-(4'-formyl-phenyl)propanoate 
• 113850-76-3 N-(tert-butoxycarbonyl)-4-iodo-L-phenylalanine methyl ester 
• 112766-18-4 methyl N-(tert-butoxycarbonyl)-O-[(trifluoromethyl)sulfonyl]-L-tyrosinate 
• 15742-86-6 N-Acetyl (4-hydroxymethyl)-DL-phenylalanine 
• 1991-87-3 4-methyl-L-phenylalanine 

Downstream Products

• 216774-50-4 N-tert-butyloxycarbonyl-(p-hydroxymethyl)-L-phenylalanine methyl ester 
• 216774-45-7 methyl 2-(S)-((tert-butoxycarbonyl)amino)-3-(4'-formyl-phenyl)propanoate 
• 206060-45-9 N-(fluorenyl-9-methoxycarbonyl)-L-(p-sulfomethyl)phenylalanine 
• 945245-47-6 N-(fluorenyl-9-methoxycarbonyl)-L-(p-sulfomethyl)phenylalanine methyl ester 
• 945245-46-5 N-(fluorenyl-9-methoxycarbonyl)-L-(p-bromomethyl)phenylalanine methyl ester 
• 945245-45-4 N-(fluorenyl-9-methoxycarbonyl)-L-(p-hydroxymethyl)phenylalanine methyl ester 
• 945245-54-5 N-(fluorenyl-9-methoxycarbonyl)-L-(p-sulfomethyl)phenylalanyl-L-(4-O-benzyl)-aspartic acid α-tert-butyl ester 

Relevant articles and documents

(p-Sulfomethyl)phenylalanine as a mimic of O-sulfatyl-tyrosine in synthetic partial sequences of P-Selectin glycoprotein ligand 1 (PSGL-1)

Fmoc-l-(p-sulfomethyl)phenylalanine, a bioisosteric mimic of acid-sensitive O-sulfatyl tyrosine, was synthesized from l-tyrosine according to a novel route. Partial sequences of the recognition site of P-Selectin glycoprotein ligand 1 (PSGL-1), which cont

Synthesis of novel chiral amino acids possessing a porphyrin moiety

Phenylalanine derivatives bearing a porphyrin moiety at the para- position were prepared in an enantiomerically pure form. The synthetic nonnatural aromatic amino acid reacted with amines and acids to give novel functionalized peptides without loss of the