ChemicalBook > Product Catalog >Biochemical Engineering >Amino Acids and Derivatives >BOC-amino acid >N-Boc-L-phenylalaninal

N-Boc-L-phenylalaninal

N-Boc-L-phenylalaninal Structure
CAS No.
72155-45-4
Chemical Name:
N-Boc-L-phenylalaninal
Synonyms
BOC-PHE-CHO;N-ALPHA-T-BUT;BOC-PHE-ALDEHYDE;Boc-phenylalaninal;BOC-L-PHENYLALANINAL;N-Boc-phenylalaninal;N-BOC-L-PHENYLALANINAL;N-T-BOC-L-PHENYLALANINAL;N-BOC-L-Phenylalaninal,97%;N-Boc-L-phenylalaninal 97%
CBNumber:
CB4663773
Molecular Formula:
C14H19NO3
Molecular Weight:
249.31
MOL File:
72155-45-4.mol
MSDS File:
SDS
Modify Date:
2023/7/11 8:28:09

N-Boc-L-phenylalaninal Properties

Melting point 86-88 °C (lit.)
Boiling point 367.0±35.0 °C(Predicted)
alpha -47 º (C=0.5 IN MEOH)
Density 1.077±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility Dichloromethane, Diethyl Ether
pka 11.38±0.46(Predicted)
form Solid
color White to pale brown
optical activity [α]20/D 47°, c = 0.5 in methanol
CAS DataBase Reference 72155-45-4(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P271-P280
WGK Germany  3
HS Code  29225000

N-Boc-L-phenylalaninal price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 469297 N-Boc-L-phenylalaninal 97% 72155-45-4 250MG ₹4113.5 2022-06-14 Buy
Product number Packaging Price Buy
469297 250MG ₹4113.5 Buy

N-Boc-L-phenylalaninal Chemical Properties,Uses,Production

Chemical Properties

White Solid

Uses

An amino aldehyde. A potent human cathepsin K inhibitor

N-Boc-L-phenylalaninal Preparation Products And Raw materials

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N-Boc-L-phenylalaninal Spectrum

BOC-L-PHENYLALANINAL BOC-PHE-ALDEHYDE BOC-PHE-CHO (S)-(1-BENZYL-2-OXO-ETHYL)-CARBAMIC ACID TERT-BUTYL ESTER (S)-(-)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL N-T-BOC-L-PHENYLALANINAL N-ALPHA-T-BUTOXYCARBONYL-L-PHENYALANINAL N-BOC-L-PHENYLALANINAL Boc-phenylalaninal N-(tert-Butoxycarbonyl)phenylalaninal N-[(1S)-1-Formyl-2-phenylethyl]carbamic Acid 1,1-Dimethylethyl Ester N-Boc-phenylalaninal (S)-(-)-2-(tert-butoxycarbonylamino)-3-phenylprop (S)-t-butyl 1-oxo-3-phenylpropan-2-yl carbamate (2S)-2-(tert-Butyloxycarbonylamino)-3-phenylpropanal (S)-α-(tert-Butoxycarbonylamino)benzenepropionaldehyde (αS)-α-(tert-Butyloxycarbonylamino)benzenepropanal [(S)-α-Formylphenethyl]carbamic acid tert-butyl ester N-[(S)-1-Benzyl-2-oxoethyl]carbamic acid tert-butyl ester N-BOC-L-Phenylalaninal,97% tert-butyl (R)-1-formyl-2-phenylethylcarbamate (S)-tert-butyl 1-oxo-3-phenylpropan-2-yl carbamate Carbamic acid, N-[(1S)-1-formyl-2-phenylethyl]-, 1,1-dimethylethyl ester N-Boc-L-phenylalaninal,(S)-()-2-(tert-Butoxycarbonylamino)-3-phenylpropanal N-Boc-L-phenylalaninal 97% tert-butyl(S)-(1-oxo-3-phenylpropan-2-yl)carbamate N-Boc-2(S)-3-phenylpropanal N-ALPHA-T-BUT N-Boc-L-phenylalaninal USP/EP/BP N-tert-Boc-L-Phenylalaninal tert-butyl N-[(2S)-1-oxo-3-phenylpropan-2-yl]carbamate 72155-45-4 72155-45-4-8 Peptide Synthesis Specialty Synthesis Amino Aldehydes Amino Acid Derivatives Amino Acids 13C, 2H, 15N Amino Acids & Derivatives Chiral Reagents Inhibitors