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Benzene, 5-(methoxymethyl)-1,3-dimethyl-2-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40113-64-2

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40113-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40113-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,1 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40113-64:
(7*4)+(6*0)+(5*1)+(4*1)+(3*3)+(2*6)+(1*4)=62
62 % 10 = 2
So 40113-64-2 is a valid CAS Registry Number.

40113-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(methoxymethyl)-2,6-dimethylnitrobenzene

1.2 Other means of identification

Product number -
Other names 1,3-dimethyl-5-[(methyloxy)methyl]-2-nitrobenzene

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:40113-64-2 SDS

40113-64-2Relevant academic research and scientific papers

GLYCOGEN PHOSPHORYLASE INHIBITOR COMPOUND AND PHARMACEUTICAL COMPOSITION THEREOF

-

Page/Page column 9; 16, (2009/05/29)

This invention relates to a novel compound which is a glycogen phosphorylase inhibitor and its use in the treatment of diabetes and other conditions associated therewith. The invention further relates to a pharmaceutical composition containing the compoun

Migrations in Oxidations of Mesidine

Goldstein, Stephen L.,McNelis, Edward

, p. 1613 - 1620 (2007/10/02)

The oxidation of mesidine in methanolic media by ferricyanide, dichromate, and persulfate afforded an anil 4 containing a shifted methoxymethyl group in addition to the principal anil 3 formed by oxidative dealkylation.Possible intermediates 6, 7, and 8 were prepared and oxidized to the product anils.Oxidations of related anilines 9, 10, and 13 did not parallel those of mesidine but afforded analogues of 3.There is significant spectral evidence for anils with alkyl shifts but little for anils analogous to 4.

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