2177-30-2 Usage
Uses
Used in Organic Synthesis:
4,4-Dimethylpent-1-en-3-one is utilized as a key intermediate in the synthesis of various organic compounds, contributing to the development of new chemical entities and materials.
Used in Fragrance and Flavoring Industry:
Leveraging its sweet, fruity, and floral scent, 4,4-Dimethylpent-1-en-3-one is employed as a fragrance ingredient and flavoring agent in the perfumery and food industries, enhancing the sensory experience of consumer products.
Used in Pharmaceutical and Medicinal Applications:
4,4-Dimethylpent-1-en-3-one is studied for its potential pharmaceutical and medicinal properties, particularly its antimicrobial and antioxidant activities, making it a promising candidate for the development of new therapeutic agents and treatments.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 4,4-Dimethylpent-1-en-3-one is explored for its ability to inhibit the growth of various microorganisms, offering a potential alternative to conventional antibiotics in combating drug-resistant infections.
Used in Antioxidant Applications:
The antioxidant properties of 4,4-Dimethylpent-1-en-3-one make it a candidate for use in applications requiring protection against oxidative stress, such as in the development of nutraceuticals, cosmetics, and other health-related products.
Check Digit Verification of cas no
The CAS Registry Mumber 2177-30-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2177-30:
(6*2)+(5*1)+(4*7)+(3*7)+(2*3)+(1*0)=72
72 % 10 = 2
So 2177-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O/c1-5-6(8)7(2,3)4/h5H,1H2,2-4H3
2177-30-2Relevant academic research and scientific papers
Oxidation of Alkynes by Hydrogen Peroxide Catalyzed by Methylrhenium Trioxide
Zhu, Zuolin,Espenson, James H.
, p. 7728 - 7732 (2007/10/03)
The oxidation of alkynes with hydrogen peroxide is catalyzed by methylrhenium tioxide.The reactions can be rationalized by postulating that an oxirene intermediate is formed between a rhenium peroxide and the alkyne.Internal alkynes yield α-diketones and carboxylic acids, the latter from the complete cleavage of the triple bonds.Rearrangement products were observed only for aliphatic alkynes.Terminal alkynes gave carboxylic acids and their derivatives and α-keto acids as the major products, but their yields varied with the solvent used.
An Efficient and Convenient Method for the Preparation of α-Methylenated Ketones from Silyl Enol Ethers
Hayashi, Masaji,Mukaiyama, Teruaki
, p. 1283 - 1286 (2007/10/02)
In the presence of a catalytic amount of stannous halide, silyl enol ethers react with bromomethyl methyl ether to give the corresponding α-bromoethyl ketones, which are smoothly converted to α-methylenated ketones on the successive addition of tertiary amine by one-pot procedure.This method is successfully applied to a synthesis of sarkomycin intermediate.
