3299-32-9 Usage
Description
2,4,5-trimethyl-1,3-dioxolane is an organic compound belonging to the dioxolane family. It is characterized by a 1,3-dioxolane ring structure with methyl groups substituted at positions 2, 4, and 5 respectively. 2,4,5-trimethyl-1,3-dioxolane is known for its unique chemical properties and potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
2,4,5-trimethyl-1,3-dioxolane is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique ring structure and substituents make it a valuable building block for the development of new drugs with specific therapeutic properties.
Used in Chemical Synthesis:
In the field of organic chemistry, 2,4,5-trimethyl-1,3-dioxolane serves as a versatile starting material for the synthesis of a wide range of organic compounds. Its reactive functional groups allow for various chemical reactions, leading to the formation of diverse products with different applications.
Used in Flavor and Fragrance Industry:
Due to its distinct chemical structure, 2,4,5-trimethyl-1,3-dioxolane can be used as a component in the creation of unique fragrances and flavors. Its ability to contribute specific olfactory and gustatory properties makes it a valuable asset in the development of novel scents and tastes.
Used in Solvent Applications:
2,4,5-trimethyl-1,3-dioxolane's solubility properties make it suitable for use as a solvent in various chemical processes. It can be employed in the extraction, purification, and synthesis of different substances, contributing to the efficiency and effectiveness of these processes.
Used in Research and Development:
2,4,5-trimethyl-1,3-dioxolane is also utilized in research and development settings, where its unique properties can be explored for potential applications in various fields. Scientists and researchers can use this compound to study its interactions with other molecules and to develop new methodologies and techniques in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 3299-32-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3299-32:
(6*3)+(5*2)+(4*9)+(3*9)+(2*3)+(1*2)=99
99 % 10 = 9
So 3299-32-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O2/c1-4-5(2)8-6(3)7-4/h4-6H,1-3H3
3299-32-9Relevant articles and documents
ELECTROCHEMICAL CONVERSION OF 2,3-BUTANEDIOL TO ACETALDEHYDE BY OXIDATIVE CLEAVAGE BY A PERIODATE/IODATE REDOX MEDIATORY SYSTEM.
Yoshiyama,Nonaka,Baizer,Chou
, p. 201 - 206 (1985)
As electrochemical method was developed for converting 2,3-butanediol in dilute aqueous solutions to acetaldehyde by 'in cell' indirect anodic oxidation using a periodate/iodate redox mediatory system. Under optimum conditions, current efficiency for the desired acetaldehyde was close to 80% and the formation of by-products such as acetic acid, acetoin, and biacetyl was minimized or suppressed.
Acetals and Ethers. I. Sulfur Dioxide as a Catalyst in Acetal Synthesis from Aliphatic Aldehydes or Ketones and Alcohols
Burczyk, Bogdan
, p. 173 - 176 (2007/10/02)
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