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62038-48-6

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62038-48-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62038-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,3 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62038-48:
(7*6)+(6*2)+(5*0)+(4*3)+(3*8)+(2*4)+(1*8)=106
106 % 10 = 6
So 62038-48-6 is a valid CAS Registry Number.

62038-48-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Dimethoxy-3,3-dimethyl-butane

1.2 Other means of identification

Product number -
Other names -

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:62038-48-6 SDS

62038-48-6Relevant articles and documents

Acetal formation from methyl formate, pinacolone, and benzophenone: equilibrium constants in methanol and water determined by a chain of transacetalization equilibria

Guthrie, J. Peter,Guo, Junan

, p. 2071 - 2076 (2007/10/02)

Transacetalization equilibrium constants can be measured in methanol solution.This allows a ladder of equilibrium constants to be constructed from acetophenone, for which the equilibrium constant for acetal formation has been measured in methanol, to methyl formate, for which it has not.This is the first direct measurement of an equilibrium constant for formation of an acetal of an acyclic ester.We have also determined equilibrium constants for acetal formation from benzophenone and pinacolone.The value for benzophenone is inconsistent with the value reported for the diethyl acetal by Pfeiffer and Adkins (G.J.Pfeiffer and H.Adkins.J.Am.Chem.Soc. 53, 1043 (1931)).We must conclude that their analytical method was subject to systematic errors.

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