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Piperidine, 1-(2,4,6-triphenyl-4H-thiopyran-4-yl)-, perchlorate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92314-72-2

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92314-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92314-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,1 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92314-72:
(7*9)+(6*2)+(5*3)+(4*1)+(3*4)+(2*7)+(1*2)=122
122 % 10 = 2
So 92314-72-2 is a valid CAS Registry Number.

92314-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,4,6-triphenyl-4H-thiopyran-4-yl)piperidine perchlorate

1.2 Other means of identification

Product number -
Other names -

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:92314-72-2 SDS

92314-72-2Relevant academic research and scientific papers

Rates and Equilibria of the Reaction of 2,4,6-Triphenylthiopyrylium Ion with Piperidine and Morpholine in Me2SO. An Unusual Proton Transfer to a Nitrogen Base

Doddi, Giancarlo,Ercolani, Gianfranco

, p. 7082 - 7087 (2007/10/02)

The complete set of kinetic and equilibrium constants of the reaction of 2,4,6-triphenylthiopyrylium ion (1) with piperidine and morpholine has been obtained in Me2SO at 25 deg C.The reaction involves the formation of both the corresponding 2H- and 4H-thiopyrans, which equilibrate to form only the more stable 2H adduct.The kinetic data are consistent with a two-step process wherein the proton transfer form the protonated 2H- and 4H-thiopyran intermediates to the amine is the rate-controlling step.The thermodynamically favored proton transfer to the neutral adducts by the solvated proton shows a rate below the diffusion limit, whwreas the observed Broensted coefficient would indicate a diffusion-controlled process.This behavior is discussed in terms of the Eigen mechanism.The factors affecting the nucleophilic addition are discussed, and a comparison is made with the previously reported reaction of 1 with primary amines.

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