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2-Cyclohexen-1-one, 2-(2-methyl-1-propenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66262-15-5

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66262-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66262-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,6 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66262-15:
(7*6)+(6*6)+(5*2)+(4*6)+(3*2)+(2*1)+(1*5)=125
125 % 10 = 5
So 66262-15-5 is a valid CAS Registry Number.

66262-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methylprop-1-enyl)cyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-(2-methyl-1-propen-1-yl)-2-cyclohexen-1-one

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:66262-15-5 SDS

66262-15-5Downstream Products

66262-15-5Relevant academic research and scientific papers

Modified stille coupling utilizing α-iodoenones

Johnson,Adams,Braun,Senanayake

, p. 919 - 922 (2007/10/02)

α-Iodoenones undergo Pd-catalyzed coupling with alkenyl- and aryltributylstannanes providing an efficient route to the corresponding α-substituted enones.

CYCLIC VINYL ETHER CARBANIONS-II PREPARATION AND APPLICATIONS TO THE SYNTHESIS OF CARBONYL COMPOUNDS

Boeckman, Robert K.,Bruza, Kenneth J.

, p. 3997 - 4006 (2007/10/02)

Conditions for metalation of a variety of cyclic vinyl ethers and reaction of the resulting carbanions with electrophiles are described.Effects of the vinyl ether structure on the relative rates of metalation are discussed.Applications of this methodology

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