4448-95-7 Usage
Uses
Used in Pharmaceutical Industry:
(3R,8aα)-2,3,4,7,8,8a-Hexahydro-4β-hydroxy-8β-(hydroxymethyl)-8α-methyl-1H-3aα,7α-methanoazulene-3β,6-dicarboxylic acid is used as a potential pharmaceutical candidate for [application reason]. Its hydroxyl and carboxylic acid groups may contribute to its bioactivity, making it a promising compound for further research and development in the pharmaceutical field.
Used in Chemical Synthesis:
(3R,8aα)-2,3,4,7,8,8a-Hexahydro-4β-hydroxy-8β-(hydroxymethyl)-8α-methyl-1H-3aα,7α-methanoazulene-3β,6-dicarboxylic acid is used as a building block in chemical synthesis for [application reason]. Its complex structure and functional groups can be utilized in the synthesis of other organic compounds, potentially leading to the development of new materials or pharmaceuticals.
Used in Research and Development:
(3R,8aα)-2,3,4,7,8,8a-Hexahydro-4β-hydroxy-8β-(hydroxymethyl)-8α-methyl-1H-3aα,7α-methanoazulene-3β,6-dicarboxylic acid is used as a subject of research and development for [application reason]. Its unique structure and potential biological activity make it an interesting compound for scientists to study and explore its properties, applications, and possible modifications to enhance its performance in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 4448-95-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4448-95:
(6*4)+(5*4)+(4*4)+(3*8)+(2*9)+(1*5)=107
107 % 10 = 7
So 4448-95-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O6/c1-14(6-16)9-5-15(11(17)4-7(9)12(18)19)8(13(20)21)2-3-10(14)15/h4,8-11,16-17H,2-3,5-6H2,1H3,(H,18,19)(H,20,21)/t8-,9-,10-,11-,14+,15+/m0/s1
4448-95-7Relevant academic research and scientific papers
Oxygenated Cedrane Derivatives : Part IV - Sodium Borohydride Reductions of Some Oxo Derivatives of Cedranoid Terpenes
Subramanian, G. B. V.,Mahajan, Vijay K.,Ganesh, K. N.
, p. 169 - 172 (2007/10/02)
Borohydride reductions of some oxygenated 9-oxo-, 10-oxo- and 8-ene-10-oxo-cedranoid terpenes are reported.While the reagent attacks preferentially from the α-face, the extent varies.The yield of the α-epimer is generally much less than that of the β-epim
