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3-Furancarbonitrile, 4,5-bis(1,3-benzodioxol-5-yl)-2-[(3-phenyl-2-propenylidene)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93665-72-6

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93665-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93665-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,6 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93665-72:
(7*9)+(6*3)+(5*6)+(4*6)+(3*5)+(2*7)+(1*2)=166
166 % 10 = 6
So 93665-72-6 is a valid CAS Registry Number.

93665-72-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-Bis-benzo[1,3]dioxol-5-yl-2-[(E)-3-phenyl-prop-2-en-(Z)-ylideneamino]-furan-3-carbonitrile

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:93665-72-6 SDS

93665-72-6Downstream Products

93665-72-6Relevant academic research and scientific papers

PREPARATION AND REACTIONS OF 2-AMINO-3-CYANO-4,5-BIS(3,4-METHYLENEDIOXYBENZYL)FURAN

Prousek, Josef

, p. 1788 - 1794 (2007/10/02)

Treatment of 2-hydroxy-1,4-bis(3,4-methylenedioxyphenyl)-3-butenone with propanedinitrile (I) catalyzed by diethylamine afforded 2-amino-3-cyano-4,5-bis(methylenedioxybenzyl)furan (II).The latter reacted with formamide to 4-amino-5,6-bis(3,4-methylenedioxybenzyl)furopyrimidine (III), and with aldehydes to the corresponding azomethines IVa-IVe.The structure of products was adduced from spectral (IR, UV, 1H NMR, and mass) data.The inhibition of incorporation of -adenine and -L-valine for DNK synthesis and proteosynthesis of leukemia P-388 cells was tested with derivatives II and III.

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