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Cyclohexane, (2-chloro-2-propenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67894-88-6

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67894-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67894-88-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,9 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67894-88:
(7*6)+(6*7)+(5*8)+(4*9)+(3*4)+(2*8)+(1*8)=196
196 % 10 = 6
So 67894-88-6 is a valid CAS Registry Number.

67894-88-6SDS

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 2-chloro-3-cyclohexylprop-1-ene

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:67894-88-6 SDS

67894-88-6Upstream product

67894-88-6Relevant academic research and scientific papers

A Cp2TiCl2-Me3Al (1:4) reagent system: An efficient reagent for generation of allylic titanocene derivatives from vinyl halides, vinyl ethers and carboxylic esters

Hanzawa, Yuji,Kowase, Noboru,Momose, Shu-Ichi,Taguchi, Takeo

, p. 11387 - 11398 (1998)

The reagent prepared in advance by stirring a mixture of a Cp'2TiCl2- Me3Al (a 1:4 ratio) reagent system in toluene for 3 days is found to be effective in generating allylic titanocene on treatment with vinyl halides, vinyl ethers and carboxylic esters in THF. The process for the generation of an allylic titanocene species from these starting materials was suggested to proceed through a formation of titanacyclobutane and the subsequent elimination of the halogen or alkoxyl group. The generated allylic titanocene intermediate was proved to be an allylic Ti(IV) species and showed the typical reactivity to carbonyl compounds.

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