14670-95-2 Usage
Uses
Used in Medicinal Chemistry:
3-BROMO-5-METHYLADAMANTANE-1-CARBOXYLIC ACID is used as a building block in the synthesis of pharmaceuticals for its unique structure and potential biological activity, which can contribute to the development of new therapeutic agents.
Used in Drug Discovery:
In the field of drug discovery, 3-BROMO-5-METHYLADAMANTANE-1-CARBOXYLIC ACID serves as a precursor, aiding in the creation of novel compounds with potential medicinal properties.
Used in Materials Science:
3-BROMO-5-METHYLADAMANTANE-1-CARBOXYLIC ACID may be utilized in materials science for its potential applications in the development of new materials or the enhancement of existing ones, thanks to its distinctive chemical structure.
Used in Organic Synthesis:
3-BROMO-5-METHYLADAMANTANE-1-CARBOXYLIC ACID is used in organic synthesis to create a variety of organic compounds, leveraging its reactive functional groups and unique molecular framework.
Further research and development are essential to fully explore and realize the wide-ranging potential applications of 3-BROMO-5-METHYLADAMANTANE-1-CARBOXYLIC ACID across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 14670-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,7 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14670-95:
(7*1)+(6*4)+(5*6)+(4*7)+(3*0)+(2*9)+(1*5)=112
112 % 10 = 2
So 14670-95-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H17BrO2/c1-10-2-8-3-11(5-10,9(14)15)7-12(13,4-8)6-10/h8H,2-7H2,1H3,(H,14,15)
14670-95-2Relevant academic research and scientific papers
FUNCTIONALIZATION OF CARBOXYLIC ACIDS OF THE ADAMANTANE AND BICYCLONONANE SERIES IN LIQUID BROMINE
Baklan, V. F.,Khil'chevskii, A. N.,Sologub, L. S.,Kukhar, V. P.
, p. 1680 - 1683 (2007/10/02)
Carboxylic acids of the adamantane and bicyclononane series react with nucleophilic reagents such as water or acetic acid in liquid bromine to give the corresponding hydroxy, acetoxy, and bromino derivatives.
