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751-35-9

751-35-9

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751-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 751-35-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 751-35:
(5*7)+(4*5)+(3*1)+(2*3)+(1*5)=69
69 % 10 = 9
So 751-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C31H23N2P/c1-4-14-24(15-5-1)34(25-16-6-2-7-17-25,26-18-8-3-9-19-26)33-32-31-29-22-12-10-20-27(29)28-21-11-13-23-30(28)31/h1-23H

751-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(triphenyl-λ<sup>5</sup>-phosphanylidene)amino]fluoren-9-imine

1.2 Other means of identification

Product number -
Other names 9-fluorenone triphenylphosphazine

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:751-35-9 SDS

751-35-9Relevant articles and documents

Dimers of the 9-Diazofluorene Anion Radical and Their Behavior

Bethell, Donald,Parker, Vernon D.

, p. 895 - 900 (1986)

Derivative cyclic voltammetry (DCV) has been used to investigate further the dimeric species formed when 9-diazofluorene undergoes one-electron reduction in acetonitrile solution.It has been confirmed that, at low substrate concentration (0.25 mM), the an

A Kinetic Study of the Reaction of Diazoalkanes with Triphenylphosphine: Structure and Reactivity in a Biphilic Process

Bethell, Donald,Dunn, Sara F. C.,Khodaei, Medhi M.,Newall, A. Raymond

, p. 1829 - 1834 (2007/10/02)

Second-order rate coefficients and activation parameters are reported for the reaction in solution of triphenylphosphine with a series of diazoalkanes (Ar2CN2) having two aromatic groups attached to the diazo-carbon atom, 9-diazofluorene (DAF), 5-diazo-5H

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