66307-18-4 Usage
Description
1-(4-phenylpiperazin-1-yl)-3-(phenylsulfanyl)propan-2-ol is a complex organic chemical compound characterized by the presence of a piperazine ring, a sulfonyl group, and an alcohol functional group. 1-(4-phenylpiperazin-1-yl)-3-(phenylsulfanyl)propan-2-ol is known for its potential role in the synthesis of pharmaceuticals and other organic molecules due to its unique structural properties.
Uses
Used in Pharmaceutical Industry:
1-(4-phenylpiperazin-1-yl)-3-(phenylsulfanyl)propan-2-ol is used as a reagent for the synthesis of various pharmaceutical compounds. Its structural properties make it a valuable component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Organic Chemistry Research:
In the field of organic chemistry, 1-(4-phenylpiperazin-1-yl)-3-(phenylsulfanyl)propan-2-ol serves as a key intermediate in the synthesis of a wide range of organic molecules. Its versatility in forming different chemical bonds and its stability contribute to its utility in research and development.
While the provided materials do not specify particular applications or industries beyond the pharmaceutical and organic chemistry realms, the compound's structural properties suggest that it could have potential uses in other areas as well, pending further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 66307-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,0 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66307-18:
(7*6)+(6*6)+(5*3)+(4*0)+(3*7)+(2*1)+(1*8)=124
124 % 10 = 4
So 66307-18-4 is a valid CAS Registry Number.
66307-18-4Relevant articles and documents
3-Tertiary amino-1-aryloxy- or aryl-propanes and -propan -2-ols and some related compounds
Gupta,Mukerji,Chatterjee,Rastogi,Anand,Dube,Sur Jr.,Mukerji,Srimal
, p. 241 - 246 (2007/10/04)
The synthesis and pharmacological activity of some 3 tertiary amino 1 aryloxy or 1 aryl, 1 thiophenoxy and 1 anilino propan 2 ols and propanes, particularly those derived from N phenylpiperazines are described. Effect of substituents (nature/position) on the phenyl ring, the phenoxy ring as well as alteration in the hydroxylic function vis a vis the structure activity relationships (SAR) are discussed. In general, the 1 aryloxy compounds have hypotensive activity this being more pronounced in those carrying an o substituent on the phenyl ring, while m and p substituted derivatives have their effect primarily on the CNS. Variations in the phenoxy moiety do not significantly alter the intrinsic activity. The 1 aryl compounds, on the other hand, have significant CNS activity, which is markedly affected by the substituents on the 1 aryl residue.
