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3-NITROCINNAMALMALONONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41122-41-2

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41122-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41122-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,2 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 41122-41:
(7*4)+(6*1)+(5*1)+(4*2)+(3*2)+(2*4)+(1*1)=62
62 % 10 = 2
So 41122-41-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H7N3O2/c13-8-11(9-14)5-1-3-10-4-2-6-12(7-10)15(16)17/h1-7H/b3-1+

41122-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(E)-3-(3-nitrophenyl)prop-2-enylidene]propanedinitrile

1.2 Other means of identification

Product number -
Other names Malononitrile,(m-nitrocinnamylidene)

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:41122-41-2 SDS

41122-41-2Downstream Products

41122-41-2Relevant academic research and scientific papers

The clean synthesis and confirmatory structural characterization of new 2-amino-4,8-dihydropyrano[3,2-b]pyran-3-cyano based on Kojic acid

Aghbash, Khadijeh Ojaghi,Pesyan, Nader Noroozi,Notash, Behrouz

, p. 2059 - 2067 (2018)

Abstract: A valuable and clean method was developed for the synthesis of the group of different novel 2-amino-4,8-dihydropyrano[3,2-b]pyran-3-carbonitriles containing a 2-aminopyran moiety by using of azido kojic acid and various 2-arylidinemalononitriles in the presence of NH4Cl as a catalyst in a green solvent (ethanol) with excellent yields. All structures were analyzed by FT-IR, 1H, 13C NMR spectroscopy, and representatively, one compound was analyzed by X-ray crystallography technique. Crystallographic analyses indicated that of this compound a dimer formed via two weak intermolecular hydrogen bonds with d(N···O) distances of 2.927?? and made a 14-membered ring with centrosymmetric (Ci) form. Graphical abstract: [Figure not available: see fulltext.].

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