ChemicalBook > CAS DataBase List > (R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL

(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL

Product Name
(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL
CAS No.
77119-85-8
Chemical Name
(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL
Synonyms
Boc-D-Phe-aldehyde;BOC-D-PHENYLALANINAL;N-BOC-D-PHENYLALANINAL;N-T-BOC-D-PHENYLALANINAL;N-Boc-D-phenylalaninal 97%;N-BOC-D-Phenylalaninal,97%;N-Boc-2(R)-3-phenylpropanal;N-(tert-Butoxycarbonyl)-D-phenylalaninal;(R)-(+)-2-(tert-butoxycarbonylamino)-3-phenylprop;tert-butyl(R)-(1-oxo-3-phenylpropan-2-yl)carbamate
CBNumber
CB8126917
Molecular Formula
C14H19NO3
Formula Weight
249.31
MOL File
77119-85-8.mol
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(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL Property

Melting point:
86-89 °C (lit.)
storage temp. 
-20°C
form 
Crystalline Powder
color 
White or tan
optical activity
[α]20/D +45°, c = 0.5 in methanol
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Safety

WGK Germany 
3
HS Code 
29223900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H318Causes serious eye damage

Precautionary statements

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

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
469289
Product name
N-Boc-D-phenylalaninal
Purity
97%
Packaging
1g
Price
$172
Updated
2022/05/15
Biosynth Carbosynth
Product number
FB50585
Product name
Boc-D-phenylalaninal
Packaging
1g
Price
$200
Updated
2021/12/16
AK Scientific
Product number
X5488
Product name
N-Boc-D-phenylalaninal
Packaging
1g
Price
$203
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB50585
Product name
Boc-D-phenylalaninal
Packaging
250mg
Price
$80
Updated
2021/12/16
SynQuest Laboratories
Product number
4156-1-R0
Product name
N-Boc-D-Phenylalaninal
Purity
95%
Packaging
250mg
Price
$93
Updated
2021/12/16
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(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL Chemical Properties,Usage,Production

Chemical Properties

White or tan crystalline powder

Uses

Boc-D-phenylalaninal is a useful research chemical compound used as a reactant in the copper(I)-catalyzed synthesis of 1,2,3-triazoles as inhibitors of human immunodeficiency virus type 1 protease.

(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL Preparation Products And Raw materials

Raw materials

Preparation Products

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(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL Suppliers

Belgium 1 Canada 1 China 50 Germany 3 India 1 Ireland 1 Japan 1 Switzerland 1 United Kingdom 1 United States 12 Global 72
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View Lastest Price from (R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL manufacturers

Career Henan Chemical Co
Product
(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL 77119-85-8
Price
US $9.80/KG
Min. Order
1g
Purity
≥99%
Supply Ability
100kg
Release date
2020-01-10

77119-85-8, (R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANALRelated Search:

(S)-(-)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL N-BOC-L-Prolinal BOC-ARG-OH BOC-L-NORLEUCINE BOC-D-ABU-OH BOC-D-MEPHE-OH DCHA BOC-D-Phenylalanine Boc-3-(2-Naphthyl)-D-alanine BOC-D-PHENYLALANINE 4-NITROPHENYL ESTER BOC-D-4-Fluorophe (S)-N-Boc-1-Naphthylalanine N-tert-Butyloxycarbonyl-O-(2-bromobenzyloxycarbonyl)-D-tyrosine BOC-D-4-Chlorophe BOC-D-TYR(ET)-OH BOC-D-4-Nitrophe BOC-D-TYR(BZL)-OH Boc-D-Tyr-OH BOC-D-4-IODOPHENYLALANINE

  • BOC-D-PHENYLALANINAL
  • N-T-BOC-D-PHENYLALANINAL
  • N-BOC-D-PHENYLALANINAL
  • (R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL
  • (R)-(+)-2-(tert-butoxycarbonylamino)-3-phenylprop
  • N-BOC-D-Phenylalaninal,97%
  • N-Boc-D-phenylalaninal 97%
  • tert-butyl(R)-(1-oxo-3-phenylpropan-2-yl)carbamate
  • N-Boc-2(R)-3-phenylpropanal
  • tert-butyl N-[(2R)-1-oxo-3-phenylpropan-2- yl]carbaMate
  • tert-Butyl-[(2R)-1-oxo-3-phenylpropan-2-yl]carbaMat
  • N-[(2R)-1-oxo-3-phenylpropan-2-yl]carbamic acid tert-butyl ester
  • N-(tert-Butoxycarbonyl)-D-phenylalaninal
  • Carbamic acid, N-[(1R)-1-formyl-2-phenylethyl]-, 1,1-dimethylethyl ester
  • Boc-D-Phe-aldehyde
  • 77119-85-8
  • C6H5CH2CHNHCO2CCH33CHO
  • Amino Acid Derivatives
  • Amino Aldehydes
  • ALDEHYDE
  • Peptide Synthesis
  • Specialty Synthesis