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144599-95-1

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144599-95-1 Usage

Uses

N-Boc-1-Boc-L-tryptophan is generally used as a intermediate in pharmaceutical and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 144599-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,5,9 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 144599-95:
(8*1)+(7*4)+(6*4)+(5*5)+(4*9)+(3*9)+(2*9)+(1*5)=171
171 % 10 = 1
So 144599-95-1 is a valid CAS Registry Number.

144599-95-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Packaging
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  • Alfa Aesar

  • (H62542)  N-Boc-1-Boc-L-tryptophan, 95%   

  • 144599-95-1

  • 1g

  • 258.0CNY

  • Detail
  • Alfa Aesar

  • (H62542)  N-Boc-1-Boc-L-tryptophan, 95%   

  • 144599-95-1

  • 5g

  • 966.0CNY

  • Detail

144599-95-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name BOC-TRP(BOC)-OH

1.2 Other means of identification

Product number -
Other names N,N'-DI-(T-BUTYLOXYCARBONYL)-L-TRYPTOPHANE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:144599-95-1 SDS

144599-95-1Relevant articles and documents

Mild and selective deprotection of carbamates with Bu4NF

Jacquemard, Ulrich,Bénéteau, Valérie,Lefoix, Myriam,Routier, Sylvain,Mérour, Jean-Yves,Coudert, Gérard

, p. 10039 - 10047 (2007/10/03)

A new mild method allowing the removal of carbamates using TBAF in THF is reported. Reactions were performed on indole, indoline, N-methyl aniline, aniline and tryptamine derivatives. The observed selectivity according to the carbamates or the substrates is discussed. A mechanism is postulated. Graphical Abstract

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