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2-Cyclohexen-1-one, 3-ethyl-5,5-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28017-78-9

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28017-78-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28017-78-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,1 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28017-78:
(7*2)+(6*8)+(5*0)+(4*1)+(3*7)+(2*7)+(1*8)=109
109 % 10 = 9
So 28017-78-9 is a valid CAS Registry Number.

28017-78-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-5,5-dimethylcyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-Aethyl-5,5-dimethyl-cyclohex-2-enon

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:28017-78-9 SDS

28017-78-9Relevant academic research and scientific papers

Spiroannulation approach to pentalenene, an angular triquinane sesquiterpene

Wu,Zhu,Burnell

, p. 104 - 110 (1994)

The route to the angular triquinane (±)-pentalenene (1a) followed from an efficient geminal acylation of the acetal of isophorone or its homolog 6b by 1,2-bis((trimethylsilyl)oxy)cyclobutene (3) in the presence of boron trifluoride etherate. Ring cleavage

Iron Catalyzed Highly Enantioselective Epoxidation of Cyclic Aliphatic Enones with Aqueous H2O2

Cussó, Olaf,Cianfanelli, Marco,Ribas, Xavi,Klein Gebbink, Robertus J. M.,Costas, Miquel

supporting information, p. 2732 - 2738 (2016/03/12)

An iron complex with a C1-symmetric tetradentate N-based ligand catalyzes the asymmetric epoxidation of cyclic enones and cyclohexene ketones with aqueous hydrogen peroxide, providing the corresponding epoxides in good to excellent yields and enantioselectivities (up to 99% yield, and 95% ee), under mild conditions and in short reaction times. Evidence is provided that reactions involve an electrophilic oxidant, and this element is employed in performing site selective epoxidation of enones containing two alkene sites.

The coupling of butylvinyltellurides with organometallic reagents catalysed by nickel complexes

Raminelli, Cristiano,Gargalaka Jr., Jo?o,Silveira, Cláudio C.,Comasseto, Jo?o V.

, p. 8801 - 8809 (2008/02/10)

Vinylic tellurides couple efficiently with sp, sp2 and sp3 hybridised organometallic compounds (Li, MgX and Zn species) in the presence of dichloro-bis(triphenylphosphine)nickel(II) as catalyst.

Zur Photospaltung konjugierter γ,δ-Epoxyenone. UV.-Bestrahlung von 3-(1',2'-Epoxy-2'-methyl-prop-1'-yl)-5,5-dimethyl-2-cyclohexen-1-on

Weck, Guy de,Wolf, Hans Richard

, p. 224 - 234 (2007/10/02)

On 1?,?*-excitation (λ=254 nm) 9 undergoes cleavage of the C(γ),C(δ)-bond yielding 17 and a, which gives 18 by photofragmentation.In presence of maleinic ester the photolysis of 9 yields 20, in the presence of methanol 21 and 22 are

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