36979-87-0

Basic information

• Product Name: Phenylalanylmethane hydrochloride
• Synonyms: Phenylalanylmethane hydrochloride
• CAS NO: 36979-87-0
• Molecular Weight: 199.68
• Mol File: 36979-87-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Phenylalanylmethane hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: Phenylalanylmethane hydrochloride(36979-87-0)
• EPA Substance Registry System: Phenylalanylmethane hydrochloride(36979-87-0)

Safety Data

• Hazardous Substances Data: 36979-87-0(Hazardous Substances Data)

Upstream product

• 15196-02-8 (S)-3-[(benzyloxycarbonyl)amino]-1-diazo-4-phenyl-2-butanone 
• 87694-53-9 Boc-Phe-OH N,O-dimethyl hydroxamate 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 111491-96-4 (S)-3-(N-(benzyloxycarbonyl)amino)-4-phenyl-2-butanone 
• 26049-94-5 (S)-benzyl (4-chloro-3-oxo-1-phenylbutan-2-yl)carbamate 
• 85613-64-5 (S)-3-(tert-butoxycarbonyl)amino-4-phenyl-2-butanone 

Downstream Products

• 88576-79-8 Z-Ala₂-Ala-PheCH₃ 
• 88576-76-5 Z-Ala₂-PheCH₃ 
• 90427-68-2 Boc-Asp(OBz)-PheCH₃ 
• 20884-50-8 (2,4-dimethyl-5-phenylmethyl-1H-pyrrol-3-yl)ethanone 
• 88576-75-4 Ac-Ala₂-PheCH₃ 
• 88576-81-2 Boc-Asp(OH)-PheCH₃ 
• 90427-67-1 Ac-Ala₃-PheCH₃ 
• 88576-77-6 Glp-Ala₂-PheCH₃ 
• 90427-75-1 Ala₂-PheCH₃, HBr 
• 90427-69-3 Glp-Ala₃-PheCH₃ 
• 88576-78-7 Z-Glp-Ala₂-PheCH₃ 
• 90427-76-2 Ala₃-PheCH₃, HBr 
• 88576-80-1 Z-Glp-Ala₃-PheCH₃ 

Relevant articles and documents

Role of the C-terminal carboxylate in angiotensin II activity: Alcohol, ketone, and ester analogues of angiotensin II

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α-AMINO KETONES FROM AMINO ACIDS AS PRECURSORS FOR THE KNORR PYRROLE SYNTHESIS

A useful and versatile modification of the Knorr pyrrole synthesis is described.Key α-amino ketone intermediate for the Knorr condensation were readily prepared from the N-methoxy-N-methylamides of amino acids and condensed with 1,3-dicarbonyl compounds t

Thermitase - A Thermostable Serine Protease. III. Synthesis of N-Acylated Peptide Methyl Ketones as Inhibitors Reversibly Bound to the Enzyme

Methyl ketone derivatives of dipeptides to pentapeptides are used as suitable tools in the investigation of the non-covalent binding for subsite mapping of the active site of the enzyme.The synthesis is mainly performed by fragment condensation of N-acylated peptides or amino acids with methyl ketone derivatives of amino acids.These are prepared from the Z-protected chloromethyl ketones by catalytic hydrogenation.For the coupling steps the Z-protection is preferred.The peptide methyl ketones used in kinetic studies were N-protected by the Z, acetyl, Boc or pyroglutamyl residue.