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4-quinolylmethyl phenoxyethanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

274251-00-2

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274251-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 274251-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,4,2,5 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 274251-00:
(8*2)+(7*7)+(6*4)+(5*2)+(4*5)+(3*1)+(2*0)+(1*0)=122
122 % 10 = 2
So 274251-00-2 is a valid CAS Registry Number.

274251-00-2SDS

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 4-quinolylmethyl phenoxyethanoate

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:274251-00-2 SDS

274251-00-2Downstream Products

274251-00-2Relevant academic research and scientific papers

4-Quinolylmethyl and 1-naphthylmethyl as benzyl-type protecting groups of carboxylic acids removable by homogeneous palladium-catalyzed hydrogenolysis

Boutros, André,Legros, Jean-Yves,Fiaud, Jean-Claude

, p. 2239 - 2246 (2007/10/03)

4-Quinolylmethyl (4-QUI) esters are reduced by palladium-catalyzed hydrogenolysis by formate anion. The reaction conditions are compatible with reducible substituents or functional groups as aromatic bromo, alkene, aldehyde, ketone, nitrile, ethyl and benzyl esters. An allyl ester is cleaved selectively in the presence of a 4-QUI ester. 1-Naphthylmethyl (1-NAP) esters of α-amino acids could be deprotected without any racemization by the same methodology. (C) 2000 Elsevier Science Ltd.

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