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100564-78-1

100564-78-1 Structure

100564-78-1 Structure
IdentificationMore
[Name]

Boc-L-homophenylalanine
[CAS]

100564-78-1
[Synonyms]

2-tert-Butoxycarbonylamino-4-(S)-phenylbutyric acid
BOC-(+)-ALPHA-AMINO-4-PHENYLBUTYRIC ACID
BOC-HFE-OH
BOC-HOMO-L-PHENYLALANINE
BOC-HOMOPHENYLALANINE
BOC-HOMOPHE-OH
BOC-HOPHE-OH
BOC-HPH-OH
BOC-L-HOMOPHE
BOC-L-HOMOPHENYL-ALA
BOC-L-HOMOPHENYLALANINE
BOC-L-HOPHE-OH
BOC-L-HPH
BOC-L-HPHE
Boc-L-HPhe-OH
BOC-(S)-2-AMINO-4-PHENYLBUTYRIC ACID
N-ALPHA-BUTOXYCARBONYL-(+)-ALPHA-AMINO-4-PHENYLBUTYRIC ACID
N-ALPHA-T-BOC-L-HOMOPHENYLALANINE
N-ALPHA-TERT-BUTYLOXYCARBONYL-L-HOMO-PHENYLALANINE
N-BOC-(L)-HOMOPHENYLALANINE
[Molecular Formula]

C15H21NO4
[MDL Number]

MFCD00076904
[Molecular Weight]

279.33
[MOL File]

100564-78-1.mol
Chemical PropertiesBack Directory
[Melting point ]

76-80 °C
[Boiling point ]

439.6±38.0 °C(Predicted)
[density ]

1.139
[storage temp. ]

2-8°C
[solubility ]

Soluble in methanol.
[form ]

powder to crystal
[pka]

3.95±0.10(Predicted)
[color ]

White to Almost white
[Optical Rotation]

[α]20/D +6.5±1°, c = 2% in ethanol
[BRN ]

3653506
[Major Application]

peptide synthesis
[InChI]

InChI=1/C15H21NO4/c1-15(2,3)20-14(19)16-12(13(17)18)10-9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/t12-/s3
[InChIKey]

MCODLPJUFHPVQP-LBPRGKRZSA-N
[SMILES]

[C@@H](C(=O)O)(CCC1=CC=CC=C1)NC(=O)OC(C)(C)C |&1:0,r|
[CAS DataBase Reference]

100564-78-1(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
[Hazard Codes ]

Xi
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[F ]

3-10
[HazardClass ]

IRRITANT
[HS Code ]

29242990
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

White powder
[Uses]

N-Boc-L-homophenylalanine is a useful reagent for organic synthesis and other chemical processes. It is used in the preparation of piperidine-containing peptidyl proteasome inhibitors.
[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
Spectrum DetailBack Directory
[Spectrum Detail]

Boc-L-homophenylalanine(100564-78-1)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

100564-78-1(sigmaaldrich)
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