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5H-Indeno[1,2-b]pyridinium, 2,4-diphenyl-1-(phenylmethyl)-, tetrafluoroborate(1-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78019-04-2

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78019-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78019-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,1 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78019-04:
(7*7)+(6*8)+(5*0)+(4*1)+(3*9)+(2*0)+(1*4)=132
132 % 10 = 2
So 78019-04-2 is a valid CAS Registry Number.

78019-04-2SDS

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-benzyl-2,4-diphenyl-5H-indene<1,2-b>pyridiunium tetrafluoroborate

1.2 Other means of identification

Product number -
Other names N-Benzyl-6,8-diphenylindan<1,2-b>pyridinium Tetrafluoroborate

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:78019-04-2 SDS

78019-04-2Downstream Products

78019-04-2Relevant academic research and scientific papers

Kinetics and Mechanisms of Nucleophilic Displacements with Heterocycles as Leaving Groups. Part 6. Reactions of N-(Substituted Benzyl)-azaheterocyclonium Compounds with Piperidine

Katritzky, Alan R.,Basinski, Wlodzimierz H.,Ou, Yu Xiang,Musumarra, Giuseppe,Patel, Ranjan C.

, p. 1055 - 1060 (2007/10/02)

The preparation is described of series of N-(p-substituted)benzyl and N-(2-furfuryl) compounds with different heterocyclic leaving groups.First- and second-order rate constants for their reactions with piperidine in chlorobenzene are measured and discusse

Kinetics and Mechanisms of Nucleophilic Displacements with Heterocycles as Leaving Groups. 2. N-Benzylpyridinium Cations: Rate Variation with Steric Effects in the Leaving Group

Katritzky, Alan R.,El-Mowafy, Azzahra M.,Musumarra, Giuseppe,Sakizadeh, Kumars,Sana-Ullah, Choudhry,et al.

, p. 3823 - 3830 (2007/10/02)

N-Benzyl groups are transferred to piperidine from pyridinium ions by unimolecular SN1 and/or bimolecular SN2 mechanisms.Steric acceleration by α-phenyl groups is reduced by an adjacent β-methyl group but increased by constraining th

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