1392130-33-4 Usage
Description
(R)-2-((2-(hydroxydiphenylmethyl)pyrrolidin-1-yl)methyl)-6-(trifluoromethyl)phenol is a complex chiral chemical compound characterized by the presence of a pyrrolidine ring, a diphenylmethyl group, and a trifluoromethyl group attached to a phenol ring. The (R) configuration denotes its specific three-dimensional arrangement of atoms, which is crucial for its potential pharmacological properties. (R)-2-((2-(hydroxydiphenylmethyl)pyrrolidin-1-yl)methyl)-6-(trifluoromethyl)phenol is likely to have valuable applications in the pharmaceutical and research sectors due to its unique structure and functional groups.
Uses
Used in Pharmaceutical Industry:
(R)-2-((2-(hydroxydiphenylmethyl)pyrrolidin-1-yl)methyl)-6-(trifluoromethyl)phenol is used as a potential therapeutic agent for various medical conditions due to its unique chemical structure and functional groups. The presence of a phenol group allows for hydrogen bonding and other interactions that are important for biological activity. Additionally, the trifluoromethyl group enhances the metabolic stability and lipophilicity of the compound, potentially improving its pharmacokinetic properties.
Used in Research Applications:
In the field of research, (R)-2-((2-(hydroxydiphenylmethyl)pyrrolidin-1-yl)methyl)-6-(trifluoromethyl)phenol can be utilized as a starting material or a building block for the synthesis of novel compounds with potential biological activities. Its chiral nature and diverse functional groups make it an attractive candidate for the development of new drugs and other bioactive molecules.
Used in Drug Design and Optimization:
(R)-2-((2-(hydroxydiphenylmethyl)pyrrolidin-1-yl)methyl)-6-(trifluoromethyl)phenol's unique structure, including the pyrrolidinylmethyl group, may enhance its binding affinity to biological targets, making it a valuable asset in drug design and optimization processes. Researchers can leverage this property to develop more potent and selective drugs with improved efficacy and reduced side effects.
Used in Chemical Synthesis:
(R)-2-((2-(hydroxydiphenylmethyl)pyrrolidin-1-yl)methyl)-6-(trifluoromethyl)phenol can also be employed as an intermediate in the synthesis of other complex organic molecules, particularly those with potential applications in the pharmaceutical, agrochemical, or materials science industries. Its diverse functional groups and chiral nature make it a versatile building block for the creation of novel compounds with tailored properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1392130-33-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,1,3 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1392130-33:
(9*1)+(8*3)+(7*9)+(6*2)+(5*1)+(4*3)+(3*0)+(2*3)+(1*3)=134
134 % 10 = 4
So 1392130-33-4 is a valid CAS Registry Number.
1392130-33-4Relevant articles and documents
Synthesis of obscuraminol A using an organocatalyzed enantioselective Henry reaction
Filippova, Liudmila,Antonsen, Simen,Stenstr?m, Yngve,Hansen, Trond Vidar
, p. 6572 - 6577 (2016)
The first synthesis of the polyunsaturated amino alcohol natural product obscuraminol A is reported. This stereoselective synthesis was based on an anti- and enantioselective organocatalyzed Henry reaction followed by a chemoselective SmI2-mediated reduction that affected only the nitro-group of the Henry product. These efforts yielded obscuraminol A where the configuration of the all-Z skipped double bonds was conserved from the starting material, i.e. the ethyl ester of (all-Z)-eicosa-5,8,11,14,17-pentaenoic acid. Our synthesis confirmed the reported structure of obscuraminol A.
