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69775-79-7

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69775-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69775-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,7 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69775-79:
(7*6)+(6*9)+(5*7)+(4*7)+(3*5)+(2*7)+(1*9)=197
197 % 10 = 7
So 69775-79-7 is a valid CAS Registry Number.

69775-79-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2-methylpropan-2-yl)oxy]hexane

1.2 Other means of identification

Product number -
Other names Ether,hexyl t-butyl

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:69775-79-7 SDS

69775-79-7Downstream Products

69775-79-7Relevant articles and documents

Solvomercuration-Demercuration. 11. Alkoxymercuration-Demercuration of Representative Alkenes in Alcohol Solvents with the Mercuric Salts Acetate, Trifluoroacetate, Nitrate, and Methanesulfonate

Brown, Herbert C.,Kurek, Joseph T.,Rei, Min-Hon,Thompson, Kerry L.

, p. 2551 - 2557 (2007/10/02)

The alkoxymercuration-demercuration of seven representative olefins with the mercuric salts acetate, trifluoroacetate, nitrate, and methanesulfonate, in methyl, ethyl, isopropyl, and tert-butyl alcohols was examined.Mercuric acetate was effective only in methanol and ethanol.On the other hand, mercuric trifluoroacetate was effective in all four solvents, giving in most cases high yields of the corresponding ethers.Both mercuric nitrate and mercuric methanesulfonate were effective in methanol, ethanol, and 2-propanol.However, in several cases poor selectivity for the ether was observed, as evidenced by the formation of significant amounts of side products.Both electronic and steric effects are important factors in the reaction.Moreover, the structure of the olefin has a pronounced effect, both on the types of oxymercurials formed and on their stability to the reaction conditions.

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