131980-30-8

Basic information

• Product Name: BOC-L-3-CYANOPHENYLALANINE
• Synonyms: BOC-3-CYANO-L-PHENYLALANINE;BOC-L-3-CYANOPHE;BOC-L-3-CYANOPHENYLALANINE;BOC-M-CYANO-L-PHE-OH;BOC-PHE(3-CN)-OH;BOC-PHE(M-CN)-OH;(S)-N-BOC-3-CYANOPHENYLALANINE;(S)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(3-CYANOPHENYL)PROPANOIC ACID
• CAS NO: 131980-30-8
• Molecular Formula: C₁₅H₁₈N₂O₄
• Molecular Weight: 290.31
• Product Categories: Amino Acids;Phenylalanine analogs and other aromatic alpha amino acids;a-amino
• Mol File: 131980-30-8.mol
• Article Data: 8

Chemical Properties

• Melting Point: 124.1 °C
• Boiling Point: 432.4°C (rough estimate)
• Flash Point: 247.4 °C
• Appearance: /Solid
• Density: 1.1611 (rough estimate)
• Vapor Pressure: 3.09E-10mmHg at 25°C
• Refractive Index: 1.6280 (estimate)
• Storage Temp.: Store at 0°C
• PKA: 3.75±0.10(Predicted)
• CAS DataBase Reference: BOC-L-3-CYANOPHENYLALANINE(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-L-3-CYANOPHENYLALANINE(131980-30-8)
• EPA Substance Registry System: BOC-L-3-CYANOPHENYLALANINE(131980-30-8)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22
• Safety Statements: 36/37
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 131980-30-8(Hazardous Substances Data)

Usage

Chemical Properties

off-white to light yellow crystalline powder

InChI:InChI=1/C15H18N2O4/c1-15(2,3)21-14(20)17-12(13(18)19)8-10-5-4-6-11(7-10)9-16/h4-7,12H,8H2,1-3H3,(H,17,20)(H,18,19)/t12-/m1/s1

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 57213-48-6 3-cyano-(D,L)-phenylalanine 
• 74651-77-7 2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile 

Downstream Products

• 1426577-88-9 C₁₅H₂₁N₃O₅ 
• 884302-87-8 N-Boc-3'-cyano-L-phenylalanine 4-(ethoxycarbonyl)piperazinamide 
• 797040-00-7 Boc-Phe(3-AcOxam)-OH 
• 1021707-57-2 Boc-D-Phe(4-AMe)-OH*CH₃COOH 
• 216312-52-6 methyl (S)-2-((tert-butoxycarbonyl)amino)-3-(3-cyanophenyl)propanoate 
• 1354577-82-4 C₂HF₃O₂*C₄₅H₄₇N₇O₆S 
• 1354578-28-1 Boc-Phe(3-AMe-Cbz)-OH 
• 1354578-32-7 Boc-Phe(3-AMe-Cbz)-OMe 
• 1354578-34-9 C₂HF₃O₂*C₁₉H₂₂N₂O₄ 
• 1354578-35-0 C₄₄H₄₆N₄O₉S 
• 1357451-57-0 C₃₈H₄₀N₄O₇S 
• 1357451-59-2 C₃₇H₃₈N₄O₇S 
• 1354577-84-6 C₂HF₃O₂*C₄₅H₄₇N₇O₆S 
• 1354578-38-3 C₃₈H₄₀N₄O₇S 

Relevant articles and documents

SERINE PROTEASE INHIBITORS

The invention provides methods of making and using compounds of the formula shown, which are inhibitors of human plasmin and plasma kallikrein. (Formula I) The compounds are useful for the prevention of blood loss, and as components of fibrin adhesives.

N-sulphonylated amino acid derivatives, method for the production and use thereof

The present invention relates to N-sulfonylated amino acid derivatives, where an aryl radical is linked via the sulfonyl group N-terminally to the amino acid and a radical which comprises at least one imino group and at least one further basic group which

N-SULPHONYLATED AMINO ACID DERIVATIVES, METHOD FOR THE PRODUCTION AND USE THEREOF

The invention relates to N-sulphonylated amino acid derivatives wherein an aryl radical is bound to an amino acid via the sulphonyl groups in the N-terminal and a radical is bound in the C-terminal via the carbonyl group. Said radical contains at least one imino group and at least one other basic group representing an optionally modified amino-, amidino- or guanidino group. The invention also relates to a method for the production of said compounds and to the use thereof, especially as inhibitors of matriptase.