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87025-34-1

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87025-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87025-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,0,2 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87025-34:
(7*8)+(6*7)+(5*0)+(4*2)+(3*5)+(2*3)+(1*4)=131
131 % 10 = 1
So 87025-34-1 is a valid CAS Registry Number.

87025-34-1SDS

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-methoxy-2-propan-2-yloxypropane

1.2 Other means of identification

Product number -
Other names Aceton-isopropylmethylacetal

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:87025-34-1 SDS

87025-34-1Downstream Products

87025-34-1Relevant articles and documents

INDIRECT ELECTROCHEMICAL α-METHOXYLATION OF ALIPHATIC ETHERS AND ACETALS - REACTIVITY AND REGIOSELECTIVITY OF THE ANODIC OXIDATION USING TRIS(2,4-DIBROMOPHENYL)AMINE AS REDOX CATALYST

Ginzel, Klaus-Dieter,Steckhan, Eberhard,Degner, Dieter

, p. 5797 - 5806 (2007/10/02)

The technically important α-methoxylation of aliphatic ethers and acetals to form mixed acetals respectively aldehydes or ortho-esters can be performed electrochemically at low potentials in methanol solution using an undivided cell and tris(2,4-dibromophenyl)amine as redox catalyst.The regioselectivity is usually considerably higher as compared with direct electrolysis in the abscence of a catalyst.Especially valuable is the method for the regioselective methoxylation of secondary carbon atoms in presence of primary or tertiary ones and of the acetal carbon in 1,3-dioxolanes.The redox catalyst is stable under the reaction conditions so that more than thousand turnovers could be obtained.

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