31061-65-1 Usage
Description
Tricyclo[4.3.1.1^3,8^]undecane-1-carboxylic acid is a bicyclic organic compound with the molecular formula C11H16O2. It features a rigid tricyclic backbone and a carboxylic acid group attached to one of the carbon atoms. tricyclo[4.3.1.1~3,8~]undecane-1-carboxylic acid is not commonly found in nature but can be synthesized in the laboratory for research purposes.
Uses
Used in Organic Chemistry:
Tricyclo[4.3.1.1^3,8^]undecane-1-carboxylic acid is used as a reactant in various organic chemistry reactions, taking advantage of its unique tricyclic structure and carboxylic acid group for the synthesis of other complex molecules.
Used in Pharmaceutical Research:
Due to its distinctive structure, tricyclo[4.3.1.1^3,8^]undecane-1-carboxylic acid is used as a building block in the synthesis of pharmaceutical compounds. Its potential applications in drug development are currently under investigation.
Used in Material Science Research:
The rigid tricyclic backbone of tricyclo[4.3.1.1^3,8^]undecane-1-carboxylic acid makes it an interesting target for material science research. It may be utilized in the development of new materials with specific properties, such as improved stability or unique interactions with other molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 31061-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,6 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 31061-65:
(7*3)+(6*1)+(5*0)+(4*6)+(3*1)+(2*6)+(1*5)=71
71 % 10 = 1
So 31061-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O2/c13-11(14)12-5-8-1-2-9(6-12)4-10(3-8)7-12/h8-10H,1-7H2,(H,13,14)
31061-65-1Relevant articles and documents
The Isomerisation of Homoadamantane-3-carboxylic Acid into Homoadamantane-1-carboxylic Acid
Langhals, Heinz,Mergelsberg, Ingrid,Ruechardt, Christoph,Burger, Ulrich
, p. 1509 - 1524 (2007/10/02)
It is shown by D-, 13C-, and double labelling experiments that the title isomerisation 2 -> 3 under Koch-Haaf conditions is due to reversible decarbonylation followed by intermolecular hydride transfer between the bridgehead positions of the two bridgehead homoadamantane cations and homoadamantane derivatives.The isomerisation is accompanied by complete equilibration of an isotopically labelled methylene group over all possible positions.This is due to the known adamantylmethyl-3-homoadamantyl cation rearrangement which is likewise occuring.In contrast to hydride transfer reactions in the adamantyl system the methylene groups of the homoadamantyl system are not participating in the hydride transfer between the bridgehead positions.
