700-82-3 Usage
Description
3,4,5,6,7,8-hexahydro-2H-1-benzopyran-2-one, also known as Hexahydrocoumarin, is a chemical compound that is a derivative of Coumarin. It is characterized by its unique structure and properties, making it a versatile molecule for various applications.
Uses
Used in Fragrance Industry:
3,4,5,6,7,8-hexahydro-2H-1-benzopyran-2-one is used as a fragrance ingredient for its aromatic properties. It provides a pleasant scent to various products, such as perfumes, cosmetics, and personal care items.
Used in Pharmaceutical Industry:
3,4,5,6,7,8-hexahydro-2H-1-benzopyran-2-one is used as an active pharmaceutical ingredient for its potential therapeutic effects. Its unique structure allows it to interact with biological targets, making it a promising candidate for the development of new drugs.
Used in Chemical Research:
3,4,5,6,7,8-hexahydro-2H-1-benzopyran-2-one is used as a research compound in various scientific studies. Its unique properties make it an interesting subject for research, allowing scientists to explore its potential applications and mechanisms of action.
Used in Material Science:
3,4,5,6,7,8-hexahydro-2H-1-benzopyran-2-one is used in the development of new materials with specific properties. Its unique structure and chemical properties make it a valuable component in the creation of advanced materials for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 700-82-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 700-82:
(5*7)+(4*0)+(3*0)+(2*8)+(1*2)=53
53 % 10 = 3
So 700-82-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O2/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H2
700-82-3Relevant articles and documents
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De Boer,Ellwanger
, p. 77,78,82 (1974)
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Studies toward the Syntheses of Functionally Substituted γ-Butyrolactones and Spiro-γ-butyrolactones and Their Reaction with Strong Acids: A Novel Route to α-Pyrones
Mandal, A.K.,Jawalkar, D.G.
, p. 2364 - 2369 (2007/10/02)
A general strategy for the conversion of 5-keto carboxylic acids, 6 (via their enol-lactones 7), to a variety of γ-lactones, 8a-c, and spiro-γ-lactones, 8d-g, is described.Lactones 8b and 8d,e may be further converted into the corresponding α-pyrones, 17b and 17d,e, respectively, in the presence of strong acids.
A VERSATILE AND CONCISE ROUTE TO FUNCTIONALLY SUBSTITUTED γ-BUTYROLACTONES AND SPIRO-γ-BUTIROLACTONES (LACTONE ANNELATION)
Mandal, Arun K.,Jawalkar, D. G.
, p. 99 - 100 (2007/10/02)
A novel route to the synthesis of functionally substituted γ-butyrolactones and spiro-γ-butyrolactones, from six-membered cyclic enol-esters, is described.
