218608-84-5

Basic information

• Product Name: BOC-(S)-3-AMINO-5-PHENYL-PENTANOIC ACID
• Synonyms: RARECHEM AK PT B053;(S)-3-(BOC-AMINO)-5-PHENYLPENTANOIC ACID;N-T-BUTOXYCARBONYL-(S)-3-AMINO-5-PHENYLPENTANOIC ACID;BOC-(S)-3-AMINO-5-PHENYL-PENTANOIC ACID;BOC-PHE(NO CH2,C*CH2)-OH;BOC-HPH-(C*CH2)OH;BOC-BETA-NVA(5-PHENYL)-OH;BOC-5-PHENYL-L-BETA-NORVALINE
• CAS NO: 218608-84-5
• Molecular Formula: C₁₆H₂₃NO₄
• Molecular Weight: 293.36
• Product Categories: 3-Amino-4-phenylbutanoic Acid Analogs;B-Amino
• Mol File: 218608-84-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 474.6°Cat760mmHg
• Flash Point: 240.8°C
• Appearance: /
• Density: 1.121g/cm³
• Vapor Pressure: 8.18E-10mmHg at 25°C
• Refractive Index: 1.521
• Storage Temp.: 2-8°C
• PKA: 4.41±0.10(Predicted)
• CAS DataBase Reference: BOC-(S)-3-AMINO-5-PHENYL-PENTANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-(S)-3-AMINO-5-PHENYL-PENTANOIC ACID(218608-84-5)
• EPA Substance Registry System: BOC-(S)-3-AMINO-5-PHENYL-PENTANOIC ACID(218608-84-5)

Safety Data

• Safety Statements: 22-24/25
• HazardClass: IRRITANT
• Hazardous Substances Data: 218608-84-5(Hazardous Substances Data)

Usage

Chemical Properties

White powder

InChI:InChI=1/C16H23NO4/c1-16(2,3)21-15(20)17-13(11-14(18)19)10-9-12-7-5-4-6-8-12/h4-8,13H,9-11H2,1-3H3,(H,17,20)(H,18,19)/t13-/m0/s1

Upstream product

• 158807-45-5 ((S)-1-Phenethyl-allyl)-carbamic acid tert-butyl ester 
• 154079-57-9 (2S,3S)-3-(tert-butoxycarbonylamino)-5-phenyl-1,2-pentanediol 
• 82732-07-8 Boc-L-homophenylalanine 
• 271600-16-9 [(S)-3-Oxo-1-phenethyl-3-((1R,2R,4R)-1,7,7-trimethyl-2-trimethylsilanyloxy-bicyclo[2.2.1]hept-2-yl)-propyl]-carbamic acid benzyl ester 
• 204577-67-3 (1R)-2-endo-acetyl-2-exo-(trimethylsilyloxy)-1,7,7-trimethylbicyclo[2.2.1]heptane 
• 748793-59-1 (4-hydroxy-4-methyl-3-oxo-1-phenethylpentyl)carbamic acid tert-butyl ester 
• 162818-40-8 (S)-3-(<(tert-butoxy)carbonyl>amino)-1-diazo-5-phenylpentan-2-one 
• 158807-48-8 [(S)-1-(2-Hydroxy-ethyl)-3-phenyl-propyl]-carbamic acid tert-butyl ester 

Downstream Products

• 158807-52-4 methyl (3S)-3-(N-tert-butoxycarbonylamino)-5-phenylpentanoate 
• 219967-74-5 (S)-3-(<<(9H-fluoren-9-yl)methoxy>carbonyl>amino)-5-phenylpentanoic acid 

Relevant articles and documents

Catalytic enantioselective conjugate addition of carbamates

Catalytic, asymmetric conjugate addition of carbamates to enoyl systems has been realized for the first time, providing a two-step access to virtually enantiopure N-protected β-amino acids. Copyright

(S)-β3-homolysine- and (S)-β3-homoserine-containing β-peptides: CD spectra in aqueous solution

For further structural studies and for physiological investigations of β-peptides, it is necessary to have H2O-soluble derivatives. Thus, we have prepared β-hexa-, β-hepta-, and β-nonapeptides (1-6) with two, three, and seven side chains of lys