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104431-32-5

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104431-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104431-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,3 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104431-32:
(8*1)+(7*0)+(6*4)+(5*4)+(4*3)+(3*1)+(2*3)+(1*2)=75
75 % 10 = 5
So 104431-32-5 is a valid CAS Registry Number.

104431-32-5SDS

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 2-(4-Nitrophenyl)-1-(5-(4-nitrophenyl)-2-furyl)ethylene

1.2 Other means of identification

Product number -
Other names 2-(4-Nitrophenyl)-1-[5-(4-nitrophenyl)-2-furyl]ethylene

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:104431-32-5 SDS

104431-32-5Downstream Products

104431-32-5Relevant articles and documents

ARYLATION OF FURAN COMPOUNDS BY ARENEDIAZONIUM SALTS

Obushak, N. D.,Ganushchak, N. I.,Lesyuk, A. I.,Dzikovskaya, L. M.,Kisilitsa, P. P.

, p. 748 - 753 (2007/10/02)

3-(5-Aryl-2-furyl)acrylic acids were obtained by the reaction of 5-arylfurfurals with malonic acid.They were arylated by diazonium salts with decarboxylation and the formation of 5-aryl-2-styrylfurans.The latter were also obtained by the interaction of furylacrolein with diazonium salts.This reaction also gave 3-(5-aryl-2-furyl)acroleins and the corresponding arylfurylacrylic acids, which were arylated again with the release of CO2 and the formation of 5-aryl-2-styrylfurans. 3-(5-Aryl-2-furyl)acroleins were also synthesized by the condensation of 5-arylfurfurals with acetaldehyde under phase-transfer conditions.The s-trans configuration of the furan ring and the exocyclic double bond were established in the obtained compounds by the PMR method.

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