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Methanone, cyclohexyl(2,5-dimethoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69210-90-8

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69210-90-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69210-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,1 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69210-90:
(7*6)+(6*9)+(5*2)+(4*1)+(3*0)+(2*9)+(1*0)=128
128 % 10 = 8
So 69210-90-8 is a valid CAS Registry Number.

69210-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexyl-(2,5-dimethoxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names 2,5-dimethoxyphenyl cyclohexyl ketone

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:69210-90-8 SDS

69210-90-8Relevant academic research and scientific papers

Friedel–Crafts reactions of acyl trifluoromethanesulfonates and cyclic acylsulfonium cations generated from acyl fluorides

Raghavendra Rao,Vallée, Yannick

, p. 4442 - 4447 (2016/07/06)

Reactive acyl trifluoromethanesulfonates are formed from the reaction of acyl fluorides with trimethylsilyl trifluoromethanesulfonate (TMSOTf). These electrophiles undergo Friedel–Crafts reactions with electron-rich aromatics at room temperature. When a sulfur atom is present at their γ position, their cyclization to acylsulfonium cations is observed and is followed by a rearrangement leading to benzothiepinones (or dibenzo[b,e]thiepinones) in 40–85% yield.

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