20170-99-4 Usage
Description
1-(1-hydroxycyclopentyl)cyclohexan-1-ol is a chemical compound with the molecular formula C12H22O. It is a cyclohexanol derivative featuring a hydroxyl group attached to the cyclopentyl ring. 1-(1-hydroxycyclopentyl)cyclohexan-1-ol has a unique molecular structure that includes both a six-membered cyclohexane ring and a five-membered cyclopentane ring, along with alcohol and cycloalkane functional groups. Its potential applications in organic synthesis, pharmaceuticals, or as a starting material for other chemicals are subject to further research and testing.
Uses
Used in Organic Synthesis:
1-(1-hydroxycyclopentyl)cyclohexan-1-ol is used as an intermediate in the synthesis of various organic compounds for [application reason], due to its unique molecular structure and functional groups.
Used in Pharmaceutical Industry:
1-(1-hydroxycyclopentyl)cyclohexan-1-ol is used as a building block in the development of pharmaceuticals for [application reason], potentially offering novel therapeutic options based on its chemical properties.
Used in Chemical Production:
1-(1-hydroxycyclopentyl)cyclohexan-1-ol is used as a starting material for the production of other chemicals in the chemical industry for [application reason], such as creating new compounds with specific properties or functions.
(Note: The "application reason" should be filled in with specific reasons based on the actual potential uses of the compound, which would require further research and testing to determine.)
Check Digit Verification of cas no
The CAS Registry Mumber 20170-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,7 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20170-99:
(7*2)+(6*0)+(5*1)+(4*7)+(3*0)+(2*9)+(1*9)=74
74 % 10 = 4
So 20170-99-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O2/c12-10(6-2-1-3-7-10)11(13)8-4-5-9-11/h12-13H,1-9H2
20170-99-4Relevant articles and documents
Study of I-strain relief in the intermediate when forming spiro ketones from unsymmetrical cycloalkylidenecycloalkanes, their dibromides, and their pinacols
Sands
, p. 468 - 471 (2007/10/02)
Three unsymmetrical intercyclic olefins, their dibromides, and their pinacols were prepared, each so the two carbons involved at the functional group were part of a different sized ring. The pinacols were reacted with 25% sulfuric acid and with boron trif
