1338245-58-1 Usage
Uses
Used in Organic Synthesis:
(3R,5R)-4-hydroxy-Tricyclo[3.3.1.13,7]decan-1-Methanol is used as a building block in organic synthesis for creating more complex molecules. Its tricyclic structure and functional groups provide a versatile platform for chemical reactions, enabling the development of novel compounds with diverse properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (3R,5R)-4-hydroxy-Tricyclo[3.3.1.13,7]decan-1-Methanol may be utilized as an intermediate in the synthesis of pharmaceutical compounds. Its unique stereochemistry and functional groups could contribute to the development of new drugs with specific therapeutic effects.
Used in Research and Development:
(3R,5R)-4-hydroxy-Tricyclo[3.3.1.13,7]decan-1-Methanol serves as a valuable compound in research and development settings. Its distinctive structure and properties make it an interesting subject for scientific studies aimed at understanding its potential uses and optimizing its synthesis for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1338245-58-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,2,4 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1338245-58:
(9*1)+(8*3)+(7*3)+(6*8)+(5*2)+(4*4)+(3*5)+(2*5)+(1*8)=161
161 % 10 = 1
So 1338245-58-1 is a valid CAS Registry Number.
1338245-58-1Relevant academic research and scientific papers
Microbiological Hydroxylation of Some Adamantane Derivatives by Cephalosporium aphidicola
Farooq, Afgan,Hanson, James R.
, p. 150 - 151 (2007/10/03)
The sites of microbiological hydroxylation of some adamantane derivatives by Cephalosporium aphidicola, have been established.
CHARGE DISPERSAL IN 1- AND 2-ADAMANTYL CATIONS
Grob, Cyril A.,Wang, Guangyi,Yang, Chengxi
, p. 1247 - 1250 (2007/10/02)
Substituents at the remoter 5-position of 2-adamantyl arylsulfonates controlsolvolysis rates more strongly than substituents the 4-position.
