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L-Leucine, N-[(phenylmethoxy)carbonyl]-, anhydride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66414-67-3

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66414-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66414-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,1 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66414-67:
(7*6)+(6*6)+(5*4)+(4*1)+(3*4)+(2*6)+(1*7)=133
133 % 10 = 3
So 66414-67-3 is a valid CAS Registry Number.

66414-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name anhydride of N-benzyloxycarbonyl-L-valine

1.2 Other means of identification

Product number -
Other names -

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:66414-67-3 SDS

66414-67-3Relevant academic research and scientific papers

Synthesis of amino-acid derivatives of chrysin

Veselovskaya,Garazd,Ogorodniichuk,Garazd,Khilya

experimental part, p. 704 - 711 (2009/04/10)

Various conjugates of amino acids with chrysin in which the amino acid was bonded through the C- or N-terminus to the flavone were prepared using peptide chemistry methods (symmetric anhydrides and activated esters).

Amino acid derivatives of 2-R-7-hydroxy-3',4'-ethylenedioxyisoflavones

Garazd,Garazd,Aitmambetov,Khilya

, p. 301 - 304 (2007/10/03)

A number of 7-O-aminoacyl derivatives of isoflavones have been obtained by the interaction of 2-R-7-hydroxy-3′,4′-ethylenedioxyisoflavones with the symmetrical anhydrides of N-protected amino acids.

A KINETIC STUDY OF PHOSPHINIC CARBOXYLIC MIXED ANHYDRIDES

Ramage, Robert,Atrash, Butrus,Hopton, David,Parrott, Maxwell J.

, p. 1617 - 1622 (2007/10/02)

Using 32.4 MHz (31)P n.m.r. spectroscopy, disproportionation of a series of phosphinic carboxylic mixed anhydrides derived from protected α-amino acids has been studied both as a function of the substituents at phosphorus and structure of the α-amino acid being activated.It was found that the rates of disproportionation were insignificant from a preparative aspect compared with aminolysis at 0 deg C.

ACTIVATION OF A CARBOXY GROUP BY DIALKYL PYROCARBONATES. SYNTHESIS OF SYMMETRICAL ANHYDRIDES AND ARYL ESTERS OF N-PROTECTED AMINO ACIDS USING DI-tert-BUTYL PYROCARBONATE AS CONDENSING REAGENT

Pozdnev, V. F.,Chernaya, M. Yu.

, p. 333 - 337 (2007/10/02)

It has been shown that di-tert-butyl pyrocarbonate can be used as a condensing reagent in the production of anhydrides and some aryl esters of carboxylic acids.The synthesis of anhydrides and of phenyl, p-nitrophenyl, β-naphtyl, and quinolin-8-yl esters of N-protected amino acids is described.

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