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Benzoic acid, 2-benzoyl-1,2-bis(phenylmethoxy)hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38636-07-6

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38636-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38636-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,3 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38636-07:
(7*3)+(6*8)+(5*6)+(4*3)+(3*6)+(2*0)+(1*7)=136
136 % 10 = 6
So 38636-07-6 is a valid CAS Registry Number.

38636-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-Dibenzoyl-N,N'-bisbenzyloxyhydrazin

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:38636-07-6 SDS

38636-07-6Downstream Products

38636-07-6Relevant academic research and scientific papers

Electrodimerization ofN-Alkoxyamides for the Synthesis of Hydrazines

Nasier, Abudulajiang,Chang, Xihao,Guo, Chang

, p. 16068 - 16076 (2021/09/18)

An efficient and valuable N-N dimerization reaction ofN-alkoxyamides is reported under undivided electrolytic conditions. This electrochemical strategy provides a powerful way to access a wide range of advanced, highly functionalized hydrazines. Remarkably, anN-centered radical generated from the cleavage of the N-H bond under electrolytic conditions plays a crucial role in this transformation. Furthermore, variousN-alkoxyamides bearing different substituents are suitable in this transformation, furnishing the corresponding hydrazines in up to 92% yield.

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