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91759-52-3

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91759-52-3 Usage

Chemical class

Nitriles

Common uses

Ligand in catalyst preparation for organic reactions

Application field

Transition metal-catalyzed reactions

Coordination properties

Strong interaction with transition metals

Influence on catalysis

Affects selectivity and efficiency of catalytic processes

Substrate activation

Effective in promoting the transformation of various organic substrates

Value in chemistry

Valuable tool in synthetic organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 91759-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,5 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91759-52:
(7*9)+(6*1)+(5*7)+(4*5)+(3*9)+(2*5)+(1*2)=163
163 % 10 = 3
So 91759-52-3 is a valid CAS Registry Number.

91759-52-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-<(1-Phenyl-4-piperidinylidene)methyl>-1-naphthalenecarbonitrile

1.2 Other means of identification

Product number -
Other names 1-phenyl-4-[(4-cyano-1-naphthyl)methylene]piperidine

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:91759-52-3 SDS

91759-52-3Downstream Products

91759-52-3Relevant articles and documents

Synthesis and exploratory photophysical investigation of donor-bridge-acceptor systems derived from N-substituted 4-piperidones

Scherer, T.,Hielkema, W.,Krijnen, B.,Hermant, R. M.,Eijckelhoff, C.,et al.

, p. 535 - 548 (2007/10/02)

We report a two-step synthesis for N-aryl- and N-alkyl-substituted 4-piperidones, in which the N substituent can easily be varied.A number of intramolecular donor-acceptor systems was synthesized from these piperidones by conversion of the carbonyl functionality.The influence of the N-aryl donor on the electronic absorption and fluorescence spectra was investigated systematically.It was concluded that some systems can be used as efficient fluorescent probes with a high sensitivity for solvent polarity.

EXCITED-STATE DIPOLE MOMENT AND SOLVATOCHROMISM OF HIGHLY FLUORESCENT ROD-SHAPED BICHROMOPHORIC MOLECULES.

Mes,de Jong,van Ramesdonk,Verhoeven,Warman,de Haas,Horsman-van den Dool

, p. 6524 - 6528 (2007/10/02)

Efficient photoinduced charge separation can occur in molecules containing electron donor (D) and acceptor (A) groups separated by an elongated paraffinic spacer. For two molecules of this type the dipole moment of the excited state thus achieved (D** plu

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