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1H-Pyrrole-2-carboxylic acid, 4-(2-hydroxybenzoyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62484-64-4

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62484-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62484-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,8 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62484-64:
(7*6)+(6*2)+(5*4)+(4*8)+(3*4)+(2*6)+(1*4)=134
134 % 10 = 4
So 62484-64-4 is a valid CAS Registry Number.

62484-64-4SDS

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 ethyl 4-(2-hydroxybenzoyl)-1H-pyrrole-2-carboxylate

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:62484-64-4 SDS

62484-64-4Downstream Products

62484-64-4Relevant academic research and scientific papers

Synthesis of substituted pyrroles using a silver-catalysed reaction between isocyanoacetates/benzyl isocyanides and chromones

Qi, Xueyu,Xiang, Haoyue,Yang, Yuhong,Yang, Chunhao

, p. 98549 - 98552 (2015/12/04)

A novel synthetic strategy to construct substituted-pyrroles has been developed using silver-catalysed reactions between isocyanides/benzyl isocyanides and chromones. These reactions proceed under mild conditions and yield polysubstituted pyrroles with ef

Benzopyrans: Part XXIX - Reactions of some simple condensates of 4-oxo-4H-1-benzopyran-3-carboxaldehyde with nitrogen nucleophiles

Ghosh, Chandra Kanta,Sahana, Sirin,Bandyopadhyay, Chandrakanta

, p. 624 - 629 (2007/10/02)

The chromone 2, derived from the title aldehyde 1, gives the pyrazole 8 (R3 = Ph) with phenylhydrazine whereas 5 gives with H2NNHR3 (R3 =H and Ph) the pyridine derivatives (9).Hydroxylamine converts the chromones 2-4 into pyridine-1-oxides (13-15), respectively.The reaction of 1 with ethyl glycinate in the presence of pyridine affords the pyrroles 20 and 21, the former (20) being detected in the product mixture derived from 4 and ethyl glycinate.

Reactions of Formylchromone Derivatives. Part 5. Transformations of 3-Formylchromones into Pyrroles and Pyridines

Clarke, Paul D.,Fitton, Alan O.,Kosmirak, Mario,Suschitzky, Hans,Suschitzky, John L.

, p. 1747 - 1756 (2007/10/02)

4-Oxo-4H-1-benzopyran-3-carbaldehyde (3-formylchromone) (1) was treated with various bifunctional nucleophiles.With ethyl aminoethanoate it gave a mixture of ethyl 4-(2-hydroxybenzoyl)-6-(4-oxo-4H-1-benzopyran-3-yl)pyridine-2-carboxylate (2) and ethyl 4-(

TRANSFORMATION OF 3-FORMYLCHROMONES INTO PYRIDINES AND PYRROLES

Fitton, Alan O.,Kosmirak, Mario,Suschitzky, Hans,Suschitzky, John L.

, p. 3953 - 3956 (2007/10/02)

Interaction of 3-formylchromones with ethyl aminoethanoate provides a novel route to pyridines and pyrroles.

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