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Cyclohexanone, 3-(methoxymethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104681-82-5

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104681-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104681-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,8 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104681-82:
(8*1)+(7*0)+(6*4)+(5*6)+(4*8)+(3*1)+(2*8)+(1*2)=115
115 % 10 = 5
So 104681-82-5 is a valid CAS Registry Number.

104681-82-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(methoxymethyl)cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 3-(methoxymethyl)cyclohexan-1-one

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:104681-82-5 SDS

104681-82-5Downstream Products

104681-82-5Relevant academic research and scientific papers

Niacin receptor agonists, compositions containing such compounds and methods of treatment

-

Page/Page column 32; 54, (2010/11/25)

The present invention encompasses compounds of Formula I: as well as pharmaceutically acceptable salts and hydrates thereof, that are useful for treating atherosclerosis, dyslipidemias and the like. Pharmaceutical compositions and methods of use are also included.

Alcoxymethyltributyletains precurseurs d'alcoxymethyllithiums: application a la synthese de monoethers d'α-glycols et a l'homologation de cetones en aldehydes

Duchene, Alain,Mouko-Mpegna, David,Quintard, Jean-Paul

, p. 787 - 793 (2007/10/02)

Ethoxymethyltributyltin (obtained from diethoxymethyltributyltin, acetyl chloride and tributyltin hydride) and methoxymethyltributyltin (obtained from chloromethyl-methyl ether and tributylstannylmagnesium chloride) have been transmetallated with butyllithium to give the corresponding alkoxymethyl lithium reagents.This reaction, although usually performed in ether, is possible in a variety of other solvents thus simplifying some of the problems encountered during isolation of the products.The alkoxymethyllithiums obtained react with aldehydes and ketones to give cleanly the corresponding monoprotected α-glycols.Stereochemical trends were observed for hydratropaldehyde and 4-tertiarybutylcyclohexanone, while regiochemical trends were evaluated in the case of cyclohexen-2-one.Syntheis of aldehydes has been achieved in good yields from tertiary monoprotected α-glycols using conventional methods.

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