(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