757124-25-7 Usage
Chemical class
Amines
Explanation
The compound belongs to the class of amines, which are organic compounds containing nitrogen atoms with a single bond to carbon or hydrogen.
Explanation
The compound has a unique structure with two rings, a cyclobutane ring (four-membered carbon ring) fused to a pentalene ring (a type of polycyclic aromatic hydrocarbon with five carbons in the ring).
Explanation
The prefix "octahydro" indicates that the compound contains six saturated carbon atoms, meaning these carbon atoms are bonded to the maximum number of hydrogen atoms possible (four bonds per carbon).
Explanation
Due to its unique structure, the compound may have potential applications in various fields, such as organic synthesis (creating new compounds), pharmaceuticals (developing new drugs), or materials science (creating new materials with specific properties).
Explanation
To fully understand the compound's properties and potential uses, additional research would be required, as the information provided is limited and does not cover all aspects of the compound's behavior or applicability.
Bicyclic structure
Cyclobutane ring fused to a pentalene ring
Octahydro prefix
Six saturated carbon atoms
Potential applications
Organic synthesis, pharmaceuticals, materials science
Further research needed
Specific properties and potential uses
Check Digit Verification of cas no
The CAS Registry Mumber 757124-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,7,1,2 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 757124-25:
(8*7)+(7*5)+(6*7)+(5*1)+(4*2)+(3*4)+(2*2)+(1*5)=167
167 % 10 = 7
So 757124-25-7 is a valid CAS Registry Number.
757124-25-7Relevant academic research and scientific papers
Selective reductive dimerization of homocubane series oximes
Rodionov,Sklyarova,Shamota,Schreiner,Fokin
body text, p. 1695 - 1702 (2012/03/12)
The mixture of di- and monoethylene ketals obtained by the reaction of 1,9-dibromopentacyc lo[5.4.0.02,6.03,10.0 5,9]-undeca-8,11-dione followed by hydrolysis and ring contraction by Faworsky method was converted into a mixture of ethylene ketals of 7-bromopentacyclo[5.3.0.02,5.03,9.04,8]decan-6- one-4- and 5-bromopentacyclo[5.3.0.02,5.03,9.0 4,8]decan-6-one-8-carboxylic acid where the carboxy group was replaced by bromine along the procedure of Hunsdiecker-Borodine-Cristol. 6-Ethylene ketal of the pentacyclo[5.3.0.02,5.03,9.0 4,8] decan-6-one obtained by the debromination of ethylene ketals of 4,7- and 5,8-dibromopentacyclo[5.3.0.02,5.03,9.0 4,8] decan-6-one was hydrolyzed to ketone whose oxime was selectively reduced on a platinum catalyst into the di-6-pentacyclo[5.3.0.0 2,5.03,9.04,8]decylamine. The reaction of reductive dimerization was also characteristic of pentacyclo[4.3.0.0 2,5.03,8.04,7]-nonan-9-one and pentacyclo[6.3.0.02,6.03,10.05,9]undecan-4-one oximes, whereas the composition of the reduction products of pentacyclo[5.4.0.02,6.03,10.05,9]undecan-8-one oxime depended on the amount of the catalyst.
