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Cycloheptane, 1-chloro-2-(phenylthio)-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64741-06-6

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64741-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64741-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,4 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64741-06:
(7*6)+(6*4)+(5*7)+(4*4)+(3*1)+(2*0)+(1*6)=126
126 % 10 = 6
So 64741-06-6 is a valid CAS Registry Number.

64741-06-6SDS

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 trans-2-Chlor-1-cycloheptyl-phenylsulfid

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:64741-06-6 SDS

64741-06-6Relevant academic research and scientific papers

SYNTHESIS OF β-FLUOROALKYL PHENYL (OR METHYL) THIOETHERS BY SULFUR-ASSISTED HALOGEN EXCHANGE WITH TRIETHYLAMINE TRIS-HYDROFLUORIDE

Saluzzo, C.,Alvernhe, G.,Anker, D.,Haufe, G.

, p. 467 - 479 (2007/10/02)

The exchange of chlorine in β-chloroalkyl phenyl (or methyl) thioethers by fluorine, with anchimeric assistance of sulfur, is very easily realized with the almost neutral fluorinating reagent, Et3N*3HF.The 'one-pot' reactions of alkenes with sulfenyl chlo

ALKENE CARBOSULPHENYLATION AND CARBOSELENYLATION: THE USE OF ALLYLTRIMETHYLSILANE AND O-SILYLATED ENOLATES.

Alexander, Rikki P.,Paterson, Ian

, p. 5911 - 5914 (2007/10/02)

Allyltrimethylsilane, as well as O-silylated enolates, can be alkylated by the PhSCl adducts of alkenes and vinyl ethers (1, X=SPh); the PhSeCl analogues (1, X=SePh), however, are less useful for alkylation purposes due to competing nucleophilic attack at selenium.

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