6331-95-9 Usage
Description
(1,3-dioxo-3,3a,7,7a-tetrahydro-4,7-epoxy-2-benzofuran-4(1H)-yl)methyl acetate is a complex organic chemical compound that is a derivative of benzofuran. It features a tetrahydrofuran ring and an epoxy group, which contribute to its potential reactivity and functionalization. The presence of an acetate group classifies it as an ester, often utilized as a protecting group for alcohols in organic synthesis. (1,3-dioxo-3,3a,7,7a-tetrahydro-4,7-epoxy-2-benzofuran-4(1H)-yl)methyl acetate holds promise in the fields of medicinal chemistry and drug discovery due to its unique structural features and potential biological activities.
Uses
Used in Organic Synthesis:
(1,3-dioxo-3,3a,7,7a-tetrahydro-4,7-epoxy-2-benzofuran-4(1H)-yl)methyl acetate is used as a building block in organic synthesis for the creation of complex organic molecules. Its structural components, including the tetrahydrofuran ring and epoxy group, allow for further reactions and modifications, making it a versatile component in the synthesis of various organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (1,3-dioxo-3,3a,7,7a-tetrahydro-4,7-epoxy-2-benzofuran-4(1H)-yl)methyl acetate is used as a starting material or intermediate in the development of new pharmaceuticals. Its potential biological and pharmacological activities, combined with its reactivity, make it a candidate for the synthesis of bioactive molecules with therapeutic applications.
Used in Drug Discovery and Development:
(1,3-dioxo-3,3a,7,7a-tetrahydro-4,7-epoxy-2-benzofuran-4(1H)-yl)methyl acetate is utilized in drug discovery and development processes to explore its potential as a lead compound or to enhance the properties of existing drug candidates. Its unique structure may offer novel mechanisms of action or improved pharmacokinetic profiles, contributing to the advancement of new therapeutic agents.
Used in the Production of Specialty Chemicals:
(1,3-dioxo-3,3a,7,7a-tetrahydro-4,7-epoxy-2-benzofuran-4(1H)-yl)methyl acetate also finds application in the production of specialty chemicals, where its specific structural features are exploited to create high-value chemical products for various industries, such as agriculture, materials science, and fragrances.
Check Digit Verification of cas no
The CAS Registry Mumber 6331-95-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6331-95:
(6*6)+(5*3)+(4*3)+(3*1)+(2*9)+(1*5)=89
89 % 10 = 9
So 6331-95-9 is a valid CAS Registry Number.
6331-95-9Relevant articles and documents
7-Oxanorbornane and norbornane mimics of a distorted β-D- mannopyranoside: Synthesis and evaluation as β-mannosidase inhibitors
Buser, Stephan,Vasella, Andrea
, p. 3151 - 3173 (2007/10/03)
The racemic 7-oxanorbornanyl and norbornanyl aminoalcohols 3, 4, 42, 45, and 46 were synthesized and tested as snail β-mannosidase inhibitors. The amino tetraol 3 was obtained from the known sulfonyl acrylate 9 and furan 10. Esterification provided 11 tha
Structure-activity relationship of cantharidin derivatives to protein phosphatases 1, 2A1, and 2B
Sodeoka, Mikiko,Baba, Yoshiyasu,Kobayashi, Satoko,Hirukawa, Nozomu
, p. 1833 - 1836 (2007/10/03)
The effects of structural modification of cantharidin on the inhibition of protein Ser/Thr phosphatases are described. Removal of the methyl substituents at C2 and C3 in cantharidin improved the inhibition of PP2B. In contrast, introduction of a substituent to C1/C4-position drastically decreased inhibition of PP1 and PP2A1. PP2B was found to be quite tolerant to modifications at the C5 position.
