119155-04-3 Usage
Uses
Used in Organic Synthesis:
ETHYL 4,5-DIMETHYL-2-FURANCARBOXYLATE is used as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure and reactivity make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ETHYL 4,5-DIMETHYL-2-FURANCARBOXYLATE is used as a building block for the development of new drugs. Its versatile chemical properties allow it to be incorporated into the molecular structures of various therapeutic agents, contributing to their efficacy and pharmacological properties.
Used in Fragrance Industry:
Due to its strong, sweet aroma, ETHYL 4,5-DIMETHYL-2-FURANCARBOXYLATE is used as a fragrance ingredient in the perfumery and cosmetics industry. It adds a pleasant scent to various products, enhancing their sensory appeal and consumer experience.
Used in Flavor Industry:
ETHYL 4,5-DIMETHYL-2-FURANCARBOXYLATE is also utilized as a flavoring agent in the food and beverage industry. Its distinctive aroma and taste profile contribute to the development of unique flavor profiles in various products, enhancing their overall flavor and consumer acceptance.
Check Digit Verification of cas no
The CAS Registry Mumber 119155-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,1,5 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 119155-04:
(8*1)+(7*1)+(6*9)+(5*1)+(4*5)+(3*5)+(2*0)+(1*4)=113
113 % 10 = 3
So 119155-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O3/c1-4-11-9(10)8-5-6(2)7(3)12-8/h5H,4H2,1-3H3
119155-04-3Relevant academic research and scientific papers
Martin, Stephen F.,Gluchowski, Charles,Campbell, Carlton L.,Chapman, Robert C.
, p. 3171 - 3180 (1988)
An efficacious, asymmetric synthesis of the 2,9-dioxabicyclononane 4 has been completed in nine chemical steps from 4,5-dimethylfuraldehyde (8).Since enantiomerically pure 4 has been previously converted in five steps by Ireland into (+)-tirandamycic acid (3) and more recently by Schlessinger into(-)-tirandamycin A(1), this achievement constitutes in a strictly formal sense the total syntheses of these substances.The key step in the synthesis of 4 features the transformation of the enantiomerically pure furfuryl diol 25 into 29 by initial selective oxidation of the furan ring and subsequent acid-catalyzed bicycloketalization.
