770-15-0 Usage
Description
BICYCLO[3.3.1]NONANE-3,7-DIONE, also known as the dioxime of bicyclo[3.3.1]nonane-3,7-dione, is a chemical compound with high stability and unique supramolecular structures formed by its syn and anti isomers. These structures exhibit distinct properties and potential applications in various fields.
Uses
Used in Chemical Industry:
BICYCLO[3.3.1]NONANE-3,7-DIONE is used as a building block for the synthesis of various complex organic molecules, taking advantage of its high stability and unique structural features.
Used in Pharmaceutical Industry:
BICYCLO[3.3.1]NONANE-3,7-DIONE is used as a starting material for the development of new drugs, due to its potential to form supramolecular structures that can interact with biological targets.
Used in Material Science:
BICYCLO[3.3.1]NONANE-3,7-DIONE is used as a component in the development of novel materials, such as supramolecular polymers and gels, leveraging its ability to form stable structures with potential applications in drug delivery and sensing.
Used in Research and Development:
BICYCLO[3.3.1]NONANE-3,7-DIONE serves as a model compound for studying the properties and behavior of supramolecular systems, contributing to the advancement of supramolecular chemistry and its applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 770-15-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 770-15:
(5*7)+(4*7)+(3*0)+(2*1)+(1*5)=70
70 % 10 = 0
So 770-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O2/c10-8-2-6-1-7(4-8)5-9(11)3-6/h6-7H,1-5H2
770-15-0Relevant articles and documents
Titanium dioxide photocatalysis of adamantane
Cermenati, Laura,Dondi, Daniele,Fagnoni, Maurizio,Albini, Angelo
, p. 6409 - 6414 (2007/10/03)
TiO2 photocatalysis of adamantane in oxygen equilibrated MeCN yields 1- and 2-adamantanol and adamantanone with limited degradation and preference for functionalization at the 1 position, particularly in the presence of silver salts. Oxidation in CH2Cl2 is less selective. The oxidation of cyclohexane and cyclododecane is slower. In N2-flushed solutions with Ag+ as a sacrificial acceptor, products from the trapping of both 1-adamantyl radical (adamantyl methyl ketone) and cation (N-adamantylacetamide) are obtained. Furthermore, alkylation of an electrophilic alkene (isopropylydenmalononitrile) has been obtained, though in a low yield.
