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17065-15-5

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17065-15-5 Usage

Physical state

Colorless to pale yellow liquid

Odor

Strong, sweet

Uses

a. Production of optical brighteners
b. Polymerization inhibitor in the production of polymers (e.g., polystyrene and polyvinyl chloride)

Environmental impact

Toxic to aquatic life

Long-term effects

May cause adverse effects in the aquatic environment

Handling and disposal

Careful handling and disposal to minimize environmental impact

Check Digit Verification of cas no

The CAS Registry Mumber 17065-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,6 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17065-15:
(7*1)+(6*7)+(5*0)+(4*6)+(3*5)+(2*1)+(1*5)=95
95 % 10 = 5
So 17065-15-5 is a valid CAS Registry Number.

17065-15-5SDS

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 1,1-Divinylcyclohexan

1.2 Other means of identification

Product number -
Other names 1,1-Divinyl-cyclohexan

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:17065-15-5 SDS

17065-15-5Relevant articles and documents

Alkylsubstituted Cyclopentanones via Hydrocarbonylating Cyclization of 1,4-Pentadiene Systems Mediated by Metal Carbonyls

Eilbracht, Peter,Acker, Michael,Totzauer, Walter

, p. 238 - 242 (2007/10/02)

3,3-Dialkyl-1,4-pentadienes 8 under the influence of metal carbonyls can be converted to unsymmetrically substituted cyclopentanones 9 by hydrocarbonylating cyclization with carbon monoxide and hydrogen or water.Starting from 1,1-divinylcycloalkanes of type 8 this method can also be used for the synthesis of spirocyclopentanones.The yields of cyclic ketones with the here used dienes are markedly better than with the unsubstituted 1,4-pentadiene itself.

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