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99142-56-0

2-Furancarboxaldehyde, 5-(2,5-dimethylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99142-56-0

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99142-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99142-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,1,4 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99142-56:
(7*9)+(6*9)+(5*1)+(4*4)+(3*2)+(2*5)+(1*6)=160
160 % 10 = 0
So 99142-56-0 is a valid CAS Registry Number.

99142-56-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2,5-dimethylphenyl)furan-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-Furancarboxaldehyde,5-(2,5-dimethylphenyl)

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:99142-56-0 SDS

99142-56-0Downstream Products

99142-56-0Relevant articles and documents

AN IMPROVED SYNTHETIC METHOD FOR 5-ARYL-2-FURANCARBALDEHYDE

D'Auria, Maurizio,Antonioletti, Roberto,Mico, Antonella De,Piancatelli, Giovanni

, p. 1575 - 1578 (2007/10/02)

An improved synthetic method for the preparation of 5-aryl-2-furancarbaldehyde via a photochemical arylation of 5-iodo-2-furancarbaldehyde is described.

Photochemical Synthesis of 3- and 5-Aryl-2-furyl Derivatives

Antonioletti, Roberto,D'Auria, Maurizio,Mico, Antonella De,Piancatelli, Giovanni,Scettri, Arrigo

, p. 1285 - 1288 (2007/10/02)

Irradiation of 3- and 5-bromofuran-2-carbaldehyde in aromatic solutions furnished, in good yield, 3- and 5-aryl-2-furyl derivatives.Analogously, 4,5-dibromofuran-2-carbaldehyde (3) and 4,5-dibromo-2-furyl methyl ketone (5) are useful starting materials for the synthesis of the previously unknown 5-aryl-4-bromo-2-furyl derivatives.Irradiation (in diethyl ether) of the above compounds furnished the debromination products in high yield.This method represents an efficient procedure for the synthesis of 4-bromofuran-2-carbaldehyde (4).

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