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66675-06-7

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66675-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66675-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,7 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66675-06:
(7*6)+(6*6)+(5*6)+(4*7)+(3*5)+(2*0)+(1*6)=157
157 % 10 = 7
So 66675-06-7 is a valid CAS Registry Number.

66675-06-7SDS

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 1-(methoxymethoxy)hexane

1.2 Other means of identification

Product number -
Other names hexyloxy-methoxy-methane

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:66675-06-7 SDS

66675-06-7Relevant articles and documents

Preparation of Formaldehyde and Acetaldehyde Acetals

Barot, Bhalchandra C.,Pinnick, Harold W.

, p. 2981 - 2983 (1981)

-

Surface-mediated solid phase reaction. Part 7. A simple and convenient procedure for the methoxymethylation of alcohols with methoxymethyl chloride on the surface of alumina

Ranu,Majee,Das

, p. 363 - 367 (2007/10/02)

A variety of alcohols react with methoxymethyl chloride on the surface of alumina without any solvent to afford the corresponding methoxymethyl ethers in good yields.

Influences on the Selectivity of the Kolbe versus the Non-Kolbe Electrolysis in the Anodic Decarboxylation of Carboxylic Acids

Klocke, Elisabeth,Matzeit, Agnes,Gockeln, Marianne,Schaefer, Hans J.

, p. 1623 - 1630 (2007/10/02)

The anodic decarboxylation of 3-oxanonanoic acid (2a) and 3-oxapentadecanoic acid (2b) in methanol leads exclusively to products of the non-Kolbe electrolysis.The influence of coelectrolysis, solvent, current density, degree of neutralization and chain length of the alkoxy group on the anodic decarboxylation of 2a, b have been investigated.An extended alkyl chain in the alkoxy group, coelectrolysis with long-chain fatty acids, ethanol or dimethylformamide as solvent, and a high current density favor the Kolbe coupling against the non-Kolbe electrolysis.Key Words: Kolbe electrolysis/ Non-Kolbe electrolysis/ Carboxylic acids, α-alkoxy-/ Solvent effects

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