17385-36-3 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
[1,1'-Bicyclohexyl]-2,2'-diol is used as a chiral auxiliary in the synthesis of pharmaceuticals and agrochemicals for its ability to influence the stereochemistry of molecules. This allows for the creation of chiral molecules with specific properties, which is crucial in the development of effective and targeted drugs and agrochemicals.
Used in Organic Synthesis:
[1,1'-Bicyclohexyl]-2,2'-diol serves as a building block in organic synthesis, contributing to the formation of complex organic compounds. Its unique structure and properties make it a valuable component in the synthesis of various organic molecules.
Used in Asymmetric Catalysis:
As a ligand in asymmetric catalysis, [1,1'-Bicyclohexyl]-2,2'-diol plays a crucial role in facilitating selective reactions that produce enantiomerically pure compounds. This is particularly important in the synthesis of chiral molecules, which often exhibit different biological activities and are essential in the development of pharmaceuticals.
It is important to handle [1,1'-Bicyclohexyl]-2,2'-diol with care, as it may pose health hazards if not properly managed. Proper safety measures should be taken to minimize any potential risks associated with its use.
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 academic research and scientific papers
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.).
