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Ethyl 2-(2,2-diMethyl-6-oxocyclohexyl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

149208-09-3

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149208-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 149208-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,2,0 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 149208-09:
(8*1)+(7*4)+(6*9)+(5*2)+(4*0)+(3*8)+(2*0)+(1*9)=133
133 % 10 = 3
So 149208-09-3 is a valid CAS Registry Number.

149208-09-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(2,2-dimethyl-6-oxocyclohexyl)acetate

1.2 Other means of identification

Product number -
Other names ethyl,2,2-dimethyl,6-oxocyclohexylacetate

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:149208-09-3 SDS

149208-09-3Relevant academic research and scientific papers

A simple synthesis of γ-cyclohomocitral

Cruz Almanza,Hinojosa Reyes

, p. 867 - 874 (1993)

A simple and efficient synthesis for γ-cyclohomocitral (10), a key and versatile intermediate for the synthesis of some furanosesquiterpenes, is described. The formal total synthesis of (±) Pallenscensone (2) was accomplished.

AN EFFICIENT SYNTHESIS OF 2-SUBSTITUTED 3,3-DIMETHYLCYCLOHEXAN-1-ONES. A SIMPLE SYNTHETIC ROUTE TO PODOCARPA-8,11,13-TRIENE INTERMEDIATES.

Banik, Bimal K.,Chakraborti, Asit K.,Ghatak, Usha Ranjan

, p. 3391 - 3397 (2007/10/02)

2-Substituted 3,3-dimethylcyclohexan-1-ones are conveniently prepared from the respective 2-substituted 3-methylcyclohex-2-en-1-ones through boron trifluoride-ether-mediated conjugate addition of a methyl group with lithium dimethylcuprate and those incorporating 2β-phenylethyl substituents have been further transformed to podocarpa-8,11,13-triene intermediates in excellent yields.

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