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6630-86-0

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6630-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6630-86-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6630-86:
(6*6)+(5*6)+(4*3)+(3*0)+(2*8)+(1*6)=100
100 % 10 = 0
So 6630-86-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H16N2O/c23-20(17-12-6-2-7-13-17)19(16-10-4-1-5-11-16)22-21-18-14-8-3-9-15-18/h1-15,21H

6630-86-0SDS

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 1,2-diphenyl-2-(phenylhydrazinylidene)ethanone

1.2 Other means of identification

Product number -
Other names Ethanedione, diphenyl-, mono(phenylhydrazone)

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:6630-86-0 SDS

6630-86-0Relevant articles and documents

An efficient tandem oxidative-protection reaction of benzylic alcohols to corresponding arylhydrazones and oximes

Badri, Rashid,Shushizadeh, Mohammad Reza

, p. 601 - 605 (2007/10/03)

A mild and efficient one-pot synthesis of hydrazones and oximes from the reaction of the oxidation product of benzyl alcohols and phenols by 3,6-bis(triphenylphosphonium)cyclohexene dichromate with phenylhydrazine, 2,4-dinitrophenylhydrazine, and hydroxylamine is described. Copyright Taylor & Francis Group, LLC.

About the Photochromic and Thermochromic Effect of Benzil Phenylhydrazones

Mueller, U.,Timpe, H.-J.,Gustav, K.

, p. 876 - 892 (2007/10/02)

Benzil phenylhydrazone 1 synthesized from benzil and phenylhydrazine possesses s-trans-E configuration detected by means of quantum chemical calculations and its spectral data.Upon irradiation a photochromic process proceeds with λ-shift Δλ ca. 80nm.The p

Oxidation of Arylhydrazones by Thallium(III) Acetate - A Kinetic Analysis of Structural Effect on the Oxidation

Balakrishnan, R.,Srinivasan, V. S.,Venkatasubramanian, N.

, p. 476 - 478 (2007/10/02)

The kinetics of oxidation of the phenylhydrazones of several substituted benzaldehydes by Tl(III) has been studied in aqueous acetic acid in the presence of initially added sodium chloride (0.05M).The reaction exhibits a first order dependence on and and is retarded by added sodium chloride and sodium acetate.The reaction is accelerated by electron-releasing substituents in the benzaldehyde moiety while electron-withdrawing substituents retard the reaction.The reaction data obey Hammett relationship with ρ = -1.62.Electron-withdrawing groups in the phenylhydrazine moiety also reduce the reaction rate (ρ = -2.66).The major product of the reaction is the cis-monohydrazone of benzil.

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