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Cyclohexane, 1,2-bis(1-methylethoxy)-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93250-28-3

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93250-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93250-28-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,5 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 93250-28:
(7*9)+(6*3)+(5*2)+(4*5)+(3*0)+(2*2)+(1*8)=123
123 % 10 = 3
So 93250-28-3 is a valid CAS Registry Number.

93250-28-3SDS

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 trans-1,2-diisopropoxycyclohexane

1.2 Other means of identification

Product number -
Other names (+-)-trans-1.2-diisopropyloxy-cyclohexane

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:93250-28-3 SDS

93250-28-3Downstream Products

93250-28-3Relevant academic research and scientific papers

Trans dialkoxylation of cyclic alkenes: A Prevost-type reaction

Schauble, J. Herman,Trauffer, Edward A.,Deshpande, Prashant P.,Evans, Robert D.

, p. 1333 - 1339 (2007/10/03)

Reaction of anhydrous silver perchlorate, sym-collidine, and iodine (2:1:1 molar ratio) with cyclic alkenes and an excess of an alcohol in CH 2Cl2 affords trans-1,2-dialkoxycycloalkanes in high yields and purity. The reaction occurs via initial formation of the trans-iodoethers, which undergo Ag-assisted iodide abstraction to give the trans-diethers. Georg Thieme Verlag Stuttgart.

MERCURY(II) OXIDE/TETRAFLUOROBORIC ACIDPROMOTED VICINAL HYDROXY- AND ALKOXYLATION OF ALKENES

Barluenga, Jose,Alonso-Cires, Luisa,Campos, Pedro J.,Asensio, Gregorio

, p. 2563 - 2568 (2007/10/02)

The reaction of alkenes with mercury(II) oxide/tetrafluoroboric acid and alcohols or water involves reduction to Hg(O) and vicinal diethers or diols are produced in good yields.Olefins bearing benzylic hydrogens in an α position lead to cinnamyl ethers.Mechanisms are proposed to account for the products and their stereochemistry.

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