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N-Boc-L-phenylalaninal

Product Name
N-Boc-L-phenylalaninal
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
Formula Weight
249.31
MOL File
72155-45-4.mol
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N-Boc-L-phenylalaninal Property

Melting point:
86-88 °C (lit.)
alpha 
-47 º (C=0.5 IN MEOH)
Boiling point:
367.0±35.0 °C(Predicted)
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)
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Safety

WGK Germany 
3
HS Code 
29225000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
469297
Product name
N-Boc-L-phenylalaninal
Purity
97%
Packaging
250mg
Price
$49
Updated
2023/06/20
Alfa Aesar
Product number
H66530
Product name
N-Boc-L-phenylalaninal, 97%
Packaging
1g
Price
$148
Updated
2023/06/20
Alfa Aesar
Product number
H66530
Product name
N-Boc-L-phenylalaninal, 97%
Packaging
250mg
Price
$44
Updated
2021/12/16
TRC
Product number
B661520
Product name
N-Boc-phenylalaninal
Packaging
500mg
Price
$1100
Updated
2021/12/16
Usbiological
Product number
262962
Product name
N-Boc-phenylalaninal
Packaging
500mg
Price
$340
Updated
2021/12/16
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N-Boc-L-phenylalaninal Chemical Properties,Usage,Production

Chemical Properties

White Solid

Uses

An amino aldehyde. A potent human cathepsin K inhibitor

Uses

Intermediate for the synthesis of hydroxyethylene dipeptide isosteres that have enzyme inhibition properties.

reaction suitability

reaction type: Boc solid-phase peptide synthesis

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

Raw materials

Preparation Products

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N-Boc-L-phenylalaninal Suppliers

Canada 2 China 121 Germany 3 India 4 Ireland 1 Japan 3 Switzerland 1 United Kingdom 6 United States 26 Global 167
Ms Life Sciences
Tel
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Fax
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Country
India
ProdList
341
Advantage
58
Pharmaffiliates Analytics and Synthetics P. Ltd
Tel
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Fax
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Email
mktg@pharmaffiliates.com
Country
India
ProdList
6739
Advantage
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A.J Chemicals
Tel
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Fax
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Email
sales@ajchem.in
Country
India
ProdList
6100
Advantage
58
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View Lastest Price from N-Boc-L-phenylalaninal manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
N-Boc-L-phenylalaninal 72155-45-4
Price
US $0.00-0.00/g
Min. Order
1g
Purity
98%min
Supply Ability
500G
Release date
2021-06-10
Career Henan Chemical Co
Product
N-Boc-L-phenylalaninal 72155-45-4
Price
US $7.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100kg
Release date
2020-01-10
Career Henan Chemical Co
Product
N-Boc-L-phenylalaninal 72155-45-4
Price
US $7.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100kg
Release date
2020-01-10

72155-45-4, N-Boc-L-phenylalaninalRelated Search:

Styrene-acrylic latex Benzoyl peroxide Benzyl alcohol 2-Chloro-2-methylpropane Benzyl acetate 1,1'-Carbonyldiimidazole Benzyl chloride Benzyl butyrate Benzyl benzoate Tris(trimethylsilyl)phosphate Phenprobamate N-(tert-Butoxycarbonyl)-L-phenylalanine N-BOC-D-PHENYLALANINAL,N-T-BOC-D-PHENYLALANINAL,BOC-D-PHENYLALANINAL N-BOC-L-Prolinal BOC-ARG-OH BOC-L-NORLEUCINE BOC-D-ABU-OH BOC-GLYCINE TERT-BUTYL ESTER

  • 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-ALPHA-T-BUT
  • N-Boc-L-phenylalaninal 97%
  • tert-butyl(S)-(1-oxo-3-phenylpropan-2-yl)carbamate
  • N-Boc-2(S)-3-phenylpropanal
  • 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