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25022-93-9

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25022-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25022-93-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,2 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25022-93:
(7*2)+(6*5)+(5*0)+(4*2)+(3*2)+(2*9)+(1*3)=79
79 % 10 = 9
So 25022-93-9 is a valid CAS Registry Number.

25022-93-9SDS

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 N-benzhydrylbenzophenone hydrazone

1.2 Other means of identification

Product number -
Other names Benzophenonbenzhydrylhydrazon

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:25022-93-9 SDS

25022-93-9Relevant articles and documents

Hypovalent Radicals. Chemical Trapping of Electrogenerated Diazoalkane Anion Radicals

Triebe, F. M.,Hawley, M. Dale,McDonald, Richard N.

, p. 574 - 575 (2007/10/02)

Diazoalkane anion radicals produced by electroreduction of diazodiphenylmethane (Ph2CN2) and 9-diazofluorene (FlN2) in the presence of certain proton donors yield the corresponding hydrazones (R2C=NNH2); formation of diphenylmethane from electroreduction of Ph2CN2 is shown to proceed by formation of the carbene anion radical Ph2C*-.

Radical Anions in the Reduction of Benzophenone Azine

Handoo, Kishan L.,Handoo, Sudesh K.

, p. 684 - 687 (2007/10/02)

Cyclic voltammetric reduction of benzophenone azine produces radical anions and dianions in two reversible one-electron steps in dimethylformamide.A similar sequence of reaction occurs when the azine is reduced with sodium naphthalenide in degassed tetrahydrofuran.ESR-spectrum is reported for the radical anion and the scope of the reaction leading to the products of electron-transfer reduction with sodium naphthalenide has been investigated.

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