10293-10-4 Usage
Uses
Used in Pharmaceutical Industry:
(+)-3,9-DIBROMOCAMPHOR is used as a chemical intermediate for the synthesis of other organic compounds, particularly in the development of new drugs for neurological disorders. Its acetylcholinesterase inhibitory activity makes it a valuable asset in the creation of medications aimed at treating such conditions.
Used in Chemical Synthesis:
In the chemical synthesis industry, (+)-3,9-DIBROMOCAMPHOR is utilized as a key component in the production of various organic compounds. Its unique structure and properties allow it to serve as a building block for the creation of complex molecules with specific applications in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 10293-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,9 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10293-10:
(7*1)+(6*0)+(5*2)+(4*9)+(3*3)+(2*1)+(1*0)=64
64 % 10 = 4
So 10293-10-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H14Br2O/c1-9-4-3-6(7(12)8(9)13)10(9,2)5-11/h6-7H,3-5H2,1-2H3/t6-,7?,9+,10?/m0/s1
10293-10-4Relevant academic research and scientific papers
Ring cleavage of camphor derivatives: formation of chiral synthons for natural products synthesis
Hutchinson, J. H.,Money, T.,Piper, S. E.
, p. 854 - 860 (2007/10/02)
Base-promoted ring cleavage of 9,10- and 8,10-dibromocamphor provides chiral intermediates for natural product synthesis.
Synthesis of 8,10-and 9,10-disubstituted camphor derivatives
Dadson, William M.,Lam, Mayda,Money, Thomas,Piper, Susan E.
, p. 343 - 346 (2007/10/02)
Regiospecific bromination and debromination reactions have been used to provide a synthetic route from camphor to optically active 8,10- and 9,10-disubstituted camphor derivatives.
