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Ethanedione, bis(4-methoxyphenyl)-, dioxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63397-13-7

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63397-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63397-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,9 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63397-13:
(7*6)+(6*3)+(5*3)+(4*9)+(3*7)+(2*1)+(1*3)=137
137 % 10 = 7
So 63397-13-7 is a valid CAS Registry Number.

63397-13-7SDS

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 N-[1,2-bis(4-methoxyphenyl)-2-nitrosoethenyl]hydroxylamine

1.2 Other means of identification

Product number -
Other names 4.4'-Dimethoxy-benzildioxim

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:63397-13-7 SDS

63397-13-7Relevant academic research and scientific papers

Oxidation of: O -dioxime by (diacetoxyiodo)benzene: Green and mild access to furoxans

He, Chunlin,Pang, Siping,Zhang, Qi,Zhang, Xun,Zhao, Cheng

, p. 1489 - 1493 (2022/01/31)

Furoxan has been widely used in the field of high energy density materials because of its excellent properties such as high density, high standard enthalpy of formation and high nitrogen content. However, its existing synthesis methods are still restricted by the problems of difficult substrate preparation and manual handling of hazardous reagents. Herein, we disclosed a mild oxidation strategy to efficiently obtain furoxan derivatives starting from readily available o-dioxime substrates. This reaction features high functional group tolerance and easy scale-up, and has excellent regioselectivity for specific nonsymmetric o-dioximes. This method greatly reduces the safety risk and simplifies the operation process, and means that diversified furoxan derivatives can be easily accessed, thus paving the way for the wide application of furoxan derivatives. This journal is

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