84319-81-3 Usage
Description
(1R,5S,7R)-3-butyl-6,7-bis(2-hydroxyphenyl)-3-azabicyclo[3.2.0]heptane-2,4-dione is a complex organic compound characterized by a bicyclic ring system, two hydroxyphenyl groups, and a butyl side chain. As a diketone, it features two ketone functional groups, and its stereochemistry is defined by the (1R,5S,7R) configuration. The presence of hydroxyphenyl groups hints at possible antioxidant or phenolic properties, while the bicyclic ring system and diketone functionality suggest unique reactivity or biological activity, indicating a wide range of potential chemical and biological applications.
Uses
Used in Pharmaceutical Industry:
(1R,5S,7R)-3-butyl-6,7-bis(2-hydroxyphenyl)-3-azabicyclo[3.2.0]heptane-2,4-dione is used as a pharmaceutical compound for its potential antioxidant or phenolic properties, which may contribute to the development of new drugs targeting various health conditions.
Used in Chemical Research:
In the field of chemical research, (1R,5S,7R)-3-butyl-6,7-bis(2-hydroxyphenyl)-3-azabicyclo[3.2.0]heptane-2,4-dione serves as a subject for studying its unique reactivity and the effects of its complex structure on chemical behavior.
Used in Material Science:
(1R,5S,7R)-3-butyl-6,7-bis(2-hydroxyphenyl)-3-azabicyclo[3.2.0]heptane-2,4-dione is utilized in material science for exploring its potential applications in the development of new materials, possibly due to its unique structural features and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 84319-81-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,1 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84319-81:
(7*8)+(6*4)+(5*3)+(4*1)+(3*9)+(2*8)+(1*1)=143
143 % 10 = 3
So 84319-81-3 is a valid CAS Registry Number.
84319-81-3Relevant articles and documents
Thermal Behavior of Head-to-head Coumarin Dimers and Their Lactone-opened Derivatives
Yonezawa, N.,Ikebe, Y.,Yoshida, T.,Hirai, T.,Saigo, K.,Hasegawa, M.
, p. 1608 - 1611 (2007/10/02)
The thermal behavior of head-to-head coumarin dimers and twelwe lactone-opened derivatives was investigated.Though the lactone rings in coumarin dimers are very susceptible to nucleophilic ring-opening, heating these derivatives reformed six-membered lactone rings except for certain imide and diamide derivatives.The large neiboring group effect allowed the relactonization by the attack of hydroxyphenyl group to carbonyl carbon in preference to the scission of cyclobutane ring.
