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41106-02-9

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41106-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41106-02-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,0 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41106-02:
(7*4)+(6*1)+(5*1)+(4*0)+(3*6)+(2*0)+(1*2)=59
59 % 10 = 9
So 41106-02-9 is a valid CAS Registry Number.

41106-02-9SDS

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 α-(2-nitrophenyl)-N-methylnitrone

1.2 Other means of identification

Product number -
Other names 2-nitro-benzaldehyde-(N-methyl oxime )

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:41106-02-9 SDS

41106-02-9Relevant articles and documents

Synthesis and application of phenyl Nitrone derivatives as acidic and microbial corrosion inhibitors

Chen, Shijun,Zhao, Kang,Chen, Gang

, (2015/06/30)

Nitrone has drawn great attention due to its wide applications as a 1,3-dipole in heterocyclic compounds synthesis and the bioactivities. With the special structure, nitrone can also be used as ligand in inorganic chemistry. Based on the current research,

One-pot synthesis and hydroxylaminolysis of asymmetrical acyclic nitrones

Coskun, Necdet,Parlar, Aydin

, p. 2445 - 2451 (2007/10/03)

Aromatic aldehydes 1 were reductively aminated to the corresponding secondary amines 2 using NaBH4 in methanol in good yields. Amines 2 were oxidized with H2O2-WO42- regioselectively to nitrones 3, the structures of which were easily determined by reacting them with hydroxylamine hydrochloride as well as by spectral means. The products of hydroxylaminolysis in ether proved to be the corresponding benzaldehyde oximes 4 and benzyl or methyl hydroxylamine hydrochlorides 5. Copyright Taylor & Francis, Inc.

An efficient and rapid chemoselective synthesis of α-Aryl-N-methylnitrones in dry media

Bigdeli,Nikje

, p. 1547 - 1549 (2007/10/03)

A simple, efficient, and eco-friendly procedure was developed for the condensation of N-methylhydroxylamine hydrochloride with benzaldehydes bearing electron-donating or electron-withdrawing substituents in the presence of powdered molecular sieves (3 A)

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