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Cyclohexanol, 2-[2-(4-methoxyphenyl)ethyl]-1,3,3-trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109988-92-3

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109988-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109988-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,9,8 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 109988-92:
(8*1)+(7*0)+(6*9)+(5*9)+(4*8)+(3*8)+(2*9)+(1*2)=183
183 % 10 = 3
So 109988-92-3 is a valid CAS Registry Number.

109988-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(4-methoxyphenyl)ethyl]-1,3,3-trimethylcyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names Cyclohexanol,2-[2-(4-methoxyphenyl)ethyl]-1,3,3-trimethyl

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:109988-92-3 SDS

109988-92-3Downstream Products

109988-92-3Relevant academic research and scientific papers

Stereoselective Total Synthesis of (+/-)-Nimbidiol

Banik, Bimal K.,Ghosh, Sukumar,Ghatak, U. R.

, p. 103 - 104 (2007/10/02)

The first total synthesis of (+/-)-nimbidiol (1), a biogenetically interesting diterpene isolated from the root bark of Azadirachta indica Linn., has been realized through the diether (8b) prepared by a simple acid-catalyzed cyclialkylation route.

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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