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

60417-85-8

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60417-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60417-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,1 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60417-85:
(7*6)+(6*0)+(5*4)+(4*1)+(3*7)+(2*8)+(1*5)=108
108 % 10 = 8
So 60417-85-8 is a valid CAS Registry Number.

60417-85-8SDS

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 3,5,5-trimethyl-2-phenylcyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-Cyclohexen-1-one,3,5,5-trimethyl-2-phenyl

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:60417-85-8 SDS

60417-85-8Downstream Products

60417-85-8Relevant academic research and scientific papers

Arynic Condensations of Ketone Enolates. 15. New Synthetic Applications of the Condensation of α,β-Unsaturated Ketone Enolates on Benzyne

Essiz, Munir,Guillaumet, Gerald,Brunet, Jean-Jacques,Caubere, Paul

, p. 240 - 246 (2007/10/02)

Arynic condensations of both cyclic and acyclic α,β-unsaturated ketone enolates are studied.First, condensation of substituted cyclohexenone enolates with benzyne leads to a new class of cyclobutanic alcohols 6.Ring opening of 6 under basic conditions is described as a good means of synthesizing benzocyclooctadienones 10 and 19, and, in appropriate cases, benzocyclooctenediones of type 12.Thermal dehydration of 6 affords 1,3-disubstituted naphthalenes in good yields.Second, condensations of a few acyclic α,β-unsaturated ketone enolates with benzyne are shown to be of synthetic usefulness; depending on the substituents on both sides of the carbonyl group, these condensations may lead either to substituted naphthalenes or to phenyl ketones or tetralones.

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