88073-01-2 Usage
Uses
Used in Fragrance and Flavor Industry:
2H-Pyran, tetrahydro-3-methyleneis used as a flavor and fragrance ingredient in a wide range of consumer products such as perfumes, soaps, and cosmetics. Its fruity odor makes it a valuable addition to these products, enhancing their sensory appeal.
Used in Pharmaceutical Industry:
2H-Pyran, tetrahydro-3-methyleneis used as a building block in the synthesis of various pharmaceutical drugs. Its unique chemical structure allows it to be a key component in the development of new medications, contributing to advancements in healthcare.
Used in Chemical Production:
2H-Pyran, tetrahydro-3-methylenealso serves as an intermediate in the production of other chemical compounds. Its versatility in chemical reactions makes it a valuable asset in the synthesis of a variety of products, further expanding its applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 88073-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,7 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88073-01:
(7*8)+(6*8)+(5*0)+(4*7)+(3*3)+(2*0)+(1*1)=142
142 % 10 = 2
So 88073-01-2 is a valid CAS Registry Number.
88073-01-2Relevant academic research and scientific papers
KINETICS AND MECHANISM OF SOME VINYL RADICAL CYCLISATIONS
Beckwith, Athelstan L.J.,O'Shea, Dennis M.
, p. 4525 - 4528 (2007/10/02)
The vinyl radicals 2a, 2b, and 11 each undergo fast exo ring closure to give 5a, 5b, and 12, the first two of which readily rearrange to ring-expanded radicals.
Homolytic Reductive Dehalogenation of Aryl and Alkyl Halides by Lithium Aluminium Hydride
Beckwith, Athelstan L. J.,Goh, Swee Hock
, p. 907 (2007/10/02)
Photochemically induced reductions by lithium aluminium hydride of various halogeno-compounds including vinyl bromides, aryl chlorides and fluorides, neophyl chloride, cyclohexyl chloride, and 7,7-dichloronorcarane in the presence of di-t-butyl peroxide afford good yields of dehalogenated products.
