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cis- and trans-1-methanesulphonyl-2-methylcyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103890-73-9

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103890-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103890-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,9 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 103890-73:
(8*1)+(7*0)+(6*3)+(5*8)+(4*9)+(3*0)+(2*7)+(1*3)=119
119 % 10 = 9
So 103890-73-9 is a valid CAS Registry Number.

103890-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name cis- and trans-1-methanesulphonyl-2-methylcyclohexane

1.2 Other means of identification

Product number -
Other names 2-methylcyclohexyl methanesulfonate

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:103890-73-9 SDS

103890-73-9Upstream product

103890-73-9Relevant academic research and scientific papers

On the mechanism of the dyotropic expansion of hydrindanes into decalins

Fall, Yagamare,Gómez, Generosa,López, Carlos Silva,Nieto Faza, Olalla,Santalla, Hugo

, p. 1073 - 1079 (2022/02/16)

A combined computational/experimental approach has revealed key mechanistic aspects in a recently reported dyotropic expansion of hydrindanes into decalins. While computer simulations had already anticipated the need for acid catalysis for making this reaction feasible under the mild conditions used in the laboratory, this work places the dyotropic step not into the reaction flask but at a later step, during the work up instead. With this information in hand the reaction has been optimized by exploring the performance of different activating agents and shown to be versatile, particularly in steroid related chemistry due to the two scaffolds that this reaction connects. Finally, the scope of the reaction has been significantly broadened by showing that this protocol can also operate in the absence of the fused six-member ring.

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