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ChemicalBook > Product Catalogue >Organic Chemistry >Carboxylic acids and derivatives >(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL

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

(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL Structure
  • ₹15003.45
  • Product name: (R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL
  • CAS: 77119-85-8
  • MF: C14H19NO3
  • MW: 249.31
  • EINECS:
  • MDL Number:MFCD00274187
  • Synonyms: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
1 prices
Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 1G
  • ManufacturerSigma-Aldrich(India)
  • Product number469289
  • Product descriptionN-Boc-D-phenylalaninal 97%
  • Packaging1G
  • Price₹15003.45
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 469289 N-Boc-D-phenylalaninal 97% 1G ₹15003.45 2022-06-14 Buy

Properties

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

Safety Information

Symbol(GHS): GHS hazard pictogramsGHS hazard pictograms
Signal word: Danger
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H302 Harmful if swallowed Acute toxicity,oral Category 4 Warning GHS hazard pictograms P264, P270, P301+P312, P330, P501
H318 Causes serious eye damage Serious eye damage/eye irritation Category 1 Danger GHS hazard pictograms P280, P305+P351+P338, P310
Precautionary statements:
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

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.

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