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51871-62-6

51871-62-6 Structure

51871-62-6 Structure
IdentificationMore
[Name]

(S)-3-(Boc-amino)-4-phenylbutyric acid
[CAS]

51871-62-6
[Synonyms]

BOC-BETA-HOMOPHENYLALANINE
BOC-BETA-HOMOPHE-OH
BOC-BETA-HOPHE-OH
BOC-BETA-HPH-OH
BOC-HOMOPHE(BETA)-OH
BOC-L-BETA-HOMOPHENYLALANINE
BOC-PHE-(C*CH2)OH
N-BETA-T-BUTOXYCARBONYL-L-BETA-HOMOPHENYLALANINE
N-T-BUTOXYCARBONYL-(S)-3-AMINO-4-PHENYLBUTYRIC ACID
(S)-3-(BOC-AMINO)-4-PHENYLBUTYRIC ACID
(S)-3-(tert-Butyloxycarbonyl)amino-4-phenylbutyric acid
(S)-BOC-B2-HOPHE-OH
(S)-BOC-BETA2-HOMOPHENYLALANINE
(S)-BOC-BETA2-HPH-OH
Boc-(S)-3-Amino-4-phenylpropionic acid
Boc-L-b-homophenylalanine
Boc-L-β-Homo-Phe-OH
Boc-L-β-homophenylalanine, HPLC 98%
BOC-SS-HOMOPHE
Boc-L-beta-HPhe-OH
[Molecular Formula]

C15H21NO4
[MDL Number]

MFCD01076271
[Molecular Weight]

279.33
[MOL File]

51871-62-6.mol
Chemical PropertiesBack Directory
[Melting point ]

101-107 °C
[Boiling point ]

444.8±38.0 °C(Predicted)
[density ]

1.139
[storage temp. ]

Store at?0-5°C
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

4.43±0.10(Predicted)
[color ]

White to Almost white
[Optical Rotation]

[α]20/D 19.0±2°, c = 1% in methylene chloride
[BRN ]

3060457
[Major Application]

peptide synthesis
[InChI]

1S/C15H21NO4/c1-15(2,3)20-14(19)16-12(10-13(17)18)9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/t12-/m0/s1
[InChIKey]

ACKWQHCPHJQANL-LBPRGKRZSA-N
[SMILES]

CC(C)(C)OC(=O)N[C@H](CC(O)=O)Cc1ccccc1
[CAS DataBase Reference]

51871-62-6(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P305+P351+P338-P337+P313-P261-P271-P304+P340-P312-P403+P233-P405-P501
[Safety Statements ]

24/25
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

29242990
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

White to off-white powder
[Uses]

peptide synthesis
[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
[Synthesis]

Chiral (S)-3-(Boc-amino)-4-phenylbutyric acid is a carboxylic organic compound, and it has been reported in the literature that chiral N-Boc-3-arylmethyl-5-oxoisoxazoles can be synthesized in a one-pot synthesis by a sequential reaction such as cross-c

Spectrum DetailBack Directory
[Spectrum Detail]

(S)-3-(Boc-amino)-4-phenylbutyric acid(51871-62-6)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

51871-62-6(sigmaaldrich)
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