17385-36-3 Usage
General Description
[1,1'-Bicyclohexyl]-2,2'-diol is a chemical compound that belongs to the class of cyclohexyl compounds. It is a white crystalline solid with a molecular formula of C12H22O2 and a molecular weight of 198.30 g/mol. [1,1'-Bicyclohexyl]-2,2'-diol is used as a chiral auxiliary in the synthesis of pharmaceuticals and agrochemicals. It can also be used as a building block in organic synthesis and as a ligand in asymmetric catalysis. The compound has potential applications in medicinal chemistry, as it can influence the stereochemistry of molecules and contribute to the creation of chiral molecules with specific properties. However, it is important to handle this compound with care, as it may pose health hazards if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 17385-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,8 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17385-36:
(7*1)+(6*7)+(5*3)+(4*8)+(3*5)+(2*3)+(1*6)=123
123 % 10 = 3
So 17385-36-3 is a valid CAS Registry Number.
17385-36-3Relevant articles and documents
Ductile Pd-Catalysed Hydrodearomatization of Phenol-Containing Bio-Oils Into Either Ketones or Alcohols using PMHS and H2O as Hydrogen Source
Di Francesco, Davide,Subbotina, Elena,Rautiainen, Sari,Samec, Joseph S. M.
supporting information, p. 3924 - 3929 (2018/09/14)
A series of phenolic bio-oil components were selectively hydrodearomatized by palladium on carbon into the corresponding ketones or alcohols in excellent yields using polymethylhydrosiloxane and water as reducing agent. The selectivity of the reaction was governed by the water concentration where selectivity to alcohol was favoured at higher water concentrations. As phenolic bio-oil examples cardanol and beech wood tar creosote were studied as substrate to the developed reaction conditions. Cardanol was hydrodearomatized into 3-pentadecylcyclohexanone in excellent yield. From beech wood tar creosote, a mixture of cyclohexanols was produced. No hydrodeoxygenation occurred, suggesting the applicability of the reported method for the production of ketone-alcohol oil from biomass. (Figure presented.).
