1933-00-2 Usage
Chemical composition
1,2-Benzenedimethanol, diformate is a chemical compound consisting of two molecules of formic acid and one molecule of 1,2-benzenedimethanol.
Classification
It is an ester, which is a type of organic compound derived from an acid and an alcohol.
Industrial applications
1,2-Benzenedimethanol, diformate is commonly used as an intermediate in the production of various plastics and resins.
Specific uses
It is utilized in the manufacturing of polyester resins, plasticizers, and coatings.
Role in specialty polymers
1,2-Benzenedimethanol, diformate is involved in the production of specialty polymers, which are high-performance materials with unique properties.
Adhesives and surfactants
It is also used as an intermediate in the synthesis of adhesives and surfactants, which are essential components in various industries.
Pharmaceutical and cosmetic industries
1,2-Benzenedimethanol, diformate serves as an intermediate in the synthesis of certain drugs and personal care products in the pharmaceutical and cosmetic sectors.
Crucial role
The compound plays a significant role in the production of a wide range of materials, contributing to the development and advancement of various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1933-00-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,3 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1933-00:
(6*1)+(5*9)+(4*3)+(3*3)+(2*0)+(1*0)=72
72 % 10 = 2
So 1933-00-2 is a valid CAS Registry Number.
1933-00-2Relevant academic research and scientific papers
Process for preparing benzylalcohols
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, (2008/06/13)
There is described an essentially two step process for the preparation of benzylalcohols including those benzylalcohols having substituents on the benzyene ring by reaction of a substituted or unsubstituted benzyl halide with a formate typically an alkali or alkaline earth metal formate to form the corresponding substituted or unsubstituted benzyl formate. In the second step of the process the benzyl formate is contacted with an alcohol whereby the same is converted into the desired benzylalcohol. Both steps can be performed employing catalysts. Described in the specification is the realization of the desired product in exceptionally high yields in a short period of time whereby the process is characterized by high space-time yields.
