63855-88-9 Usage
Uses
Used in Organic Synthesis:
Phenyl(2-phenylcyclopropyl)methanol is used as a building block in the organic synthesis industry for the production of various pharmaceutical and agrochemical products. Its unique cyclopropane ring structure makes it a valuable intermediate in the creation of chiral molecules, which are essential in the development of enantiomerically pure drugs.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, phenyl(2-phenylcyclopropyl)methanol is used as a potential anti-inflammatory and analgesic agent. Research has indicated its ability to inhibit the production of inflammatory mediators, which could contribute to the development of new treatments for inflammatory conditions and pain management.
Used in Drug Development:
Phenyl(2-phenylcyclopropyl)methanol is utilized in drug development as a key intermediate for the synthesis of chiral molecules. Its unique structural features make it a promising candidate for the creation of novel pharmaceutical compounds with improved efficacy and selectivity.
Safety Considerations:
Due to its toxic and irritant properties, phenyl(2-phenylcyclopropyl)methanol must be handled with care in all applications. Proper safety measures, including the use of personal protective equipment and adherence to hazardous substance handling protocols, are essential to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 63855-88-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,5 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63855-88:
(7*6)+(6*3)+(5*8)+(4*5)+(3*5)+(2*8)+(1*8)=159
159 % 10 = 9
So 63855-88-9 is a valid CAS Registry Number.
63855-88-9Relevant academic research and scientific papers
Preparation of aryl-substituted E-homoallylic bromides from cyclopropylcarbinol and PBr3
Roy, Sanchita,Guha, Sharmistha,Kumar Dutta, Samit,Bhar, Sanjay
, p. 1919 - 1922 (2007/10/03)
An expeditious synthesis of aryl substituted E-homoallylic bromides has been accomplished by the cleavage of cyclopropylcarbinols with phosphorus tribromide. Copyright Taylor & Francis Group, LLC.
The thionophosphate-thiolophosphate photoisomerization proceeds predominantly through a non-chain radical pathway. Synthetically viable benzylation of tetrahydrofuran, propan-2-ol and olefins
Yadav, Veejendra K.,Balamurugan, Rengarajan,Parvez, Masood,Yamdagni, Raghav
, p. 323 - 332 (2007/10/03)
The photoirradiation of thionophosphates, ROP(S)(OEt)2, derived from benzyl and vinylogously benzyl alcohols in CH3CN, with a Hanovia medium-pressure mercury lamp in a quartz vessel leads to the formation of the corresponding thiolophosphates, RSP(O)(OEt)2, through a non-chain radical pathway. This behavior of thionophosphates is unlike that of the related phosphates, which react through ionic dissociation-recombination processes. When the irradiation is conducted in solvents such as PriOH, THF and toluene, benzylation of these solvents takes place in synthetically respectable yields. Irradiation of thionophosphates in CH3CN leads to a convenient allylic benzylation of olefins.
Hypersensitive radical probe studies of Gif oxidations
Newcomb, Martin,Simakov, Pavel A.,Park, Seung-Un
, p. 819 - 822 (2007/10/03)
Hypersensitive probes were employed in mechanistic studies of Gif oxidations. The results indicate that, unlike the case in enzyme catalyzed hydroxylation reactions, diffusively free radicals are formed in Gif oxidations of these substrates.
