2896-63-1 Usage
Uses
Used in the Food Industry:
3-Propylcatechol is used as a flavoring agent for its sweet, coffee-like aroma, enhancing the taste and aroma of various food products.
Used in the Fragrance Industry:
3-Propylcatechol serves as a key component in the production of fragrances, leveraging its distinctive scent to create appealing olfactory experiences.
Used as a Chemical Intermediate:
In the chemical industry, 3-Propylcatechol is utilized as an intermediate in the synthesis of pharmaceuticals and other organic compounds, contributing to the development of new products and innovations.
Used in Antioxidant Applications:
3-Propylcatechol is recognized for its antioxidant properties, which can be harnessed to protect against oxidative stress and related conditions in various applications.
Used in Antimicrobial Applications:
3-propylcatechol's antimicrobial properties make it a potential candidate for use in products that require sanitization or preservation, such as in cosmetics or medical applications.
Used in Neurodegenerative Disease Treatment Research:
3-Propylcatechol is under investigation for its potential role in the treatment of neurodegenerative diseases, offering a promising avenue for therapeutic development.
Used in Material and Biofuel Development:
3-Propylcatechol is also being explored for its potential in the development of new materials and biofuels, reflecting its versatility and broad applicability in scientific research and industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 2896-63-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2896-63:
(6*2)+(5*8)+(4*9)+(3*6)+(2*6)+(1*3)=121
121 % 10 = 1
So 2896-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O2/c1-2-4-7-5-3-6-8(10)9(7)11/h3,5-6,10-11H,2,4H2,1H3
2896-63-1Relevant academic research and scientific papers
Synthesis of 3-Alkylcatechols via Intramolecular Cyclization
Miyakoshi, Tetsuo,Togashi, Hiroyasu
, p. 407 - 410 (2007/10/02)
The intramolecular cyclization of 2-alkanoyl-2,5-dimethoxytetrahydrofurans 4 with aqueous acid is described. 3-Alkylcatechols 7 were prepared in generally good yields by boiling the dioxane solution of compounds 4 in the presence of 1 M hydrochloric acid.In addition, 4,5-dioxoalkanals 6 were obtained in good to high yields when the dioxane solution of compounds 4 was treated with 0.1 M hydrochloric acid.
