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158694-15-6

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158694-15-6 Usage

Type of compound

dihydro derivative of isobenzofuran

Physical state

colorless, crystalline solid

Melting point

112-114°C

Usage

commonly used as an intermediate in the synthesis of various organic compounds and pharmaceuticals

Potential applications

as a monomer for producing high-performance polymers, resins, and coatings

Interest to scientific community

due to its unique chemical structure and potential for various industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 158694-15-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,6,9 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 158694-15:
(8*1)+(7*5)+(6*8)+(5*6)+(4*9)+(3*4)+(2*1)+(1*5)=176
176 % 10 = 6
So 158694-15-6 is a valid CAS Registry Number.

158694-15-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name benzene-1,2-dicarbaldehyde hydrate

1.2 Other means of identification

Product number -
Other names 1.3-Phthalandiol

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:158694-15-6 SDS

158694-15-6Downstream Products

158694-15-6Relevant articles and documents

Intramolecular Catalysis. Part 5. The Intramolecular Cannizzaro Reaction of o-Phthalaldehyde and -o-Phthalaldehyde

Bowden, Keith,El-Kaissi, Faiq A.,Ranson, Richard J.

, p. 2089 - 2092 (2007/10/02)

o-Phthalaldehyde, as well as the α,α'-dideuterio isomer, has been shown to undergo Cannizzaro reaction in water containing base, while partially hydrated and ionised.The reaction of the monoanion of the hydrate is intramolecular and of first order in the monoanion of the hydrate, and either first or zero order in the base.The rate coefficients have been measured at several temperatures and activation parameters evaluated.The kinetic isotope effect, kH/k(2)H, for the first and second order processes were found to be ca 1.9 and 1.8, respectively.The alkaline hydroly sis of the corresponding lactone, phtalide, has also been studied under the same conditions.The evidence for the intramolecular Cannizzaro reaction indicates a mechanistic pathway involving rate-determining hydride transfer from the chain tautomers of both monoanion and dianion of the hydrate.

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