194934-96-8 Usage
Uses
Used in Pharmaceutical Industry:
tert-Butyl (E)-3,5-Dihydroxy-7-[3'-(4"-fluorophenyl)-1'-methylethylindol-2'-yl)hept-6-enoate is used as an intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, including the fluorophenyl and indole moieties, makes it a valuable building block for the development of new drugs with potential applications in treating various diseases.
Used in Chemical Research:
tert-Butyl (E)-3,5-Dihydroxy-7-[3'-(4"-fluorophenyl)-1'-methylethylindol-2'-yl)hept-6-enoate is also utilized in chemical research as a model compound to study the reactivity and properties of fluorophenyl and indole-containing molecules. It can be used to investigate various reaction mechanisms and to develop new synthetic methods for the preparation of related compounds.
Used in Material Science:
Due to its structural features, tert-Butyl (E)-3,5-Dihydroxy-7-[3'-(4"-fluorophenyl)-1'-methylethylindol-2'-yl)hept-6-enoate may find applications in the field of material science, particularly in the development of new materials with specific properties, such as fluorescence or electronic properties.
Chemical Properties:
The compound is described as a white solid, indicating its appearance and physical state. Further chemical properties, such as solubility, stability, and reactivity, would need to be determined through experimental studies.
Check Digit Verification of cas no
The CAS Registry Mumber 194934-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,9,3 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 194934-96:
(8*1)+(7*9)+(6*4)+(5*9)+(4*3)+(3*4)+(2*9)+(1*6)=188
188 % 10 = 8
So 194934-96-8 is a valid CAS Registry Number.
194934-96-8Relevant academic research and scientific papers
Asymmetric synthesis of 3,5-dihydroxy-6(E)-heptenoate-containing HMG-CoA reductase inhibitors
Tempkin, Orin,Abel, Stephan,Chen, Chung-Pin,Underwood, Russell,Prasad, Kapa,Chen, Kau-Ming,Repic, Oljan,Blacklock, Thomas J.
, p. 10659 - 10670 (2007/10/03)
A 'one-pot' conversion of aldehyde 6 to hydroxyketoester 10 with high enantioselection, culminating in a practical asymmetric synthesis of (3R,5S) isomer of the antihyperlipoproteinemic agent fluvastatin, 1, is described. All four 3,5-dihydroxy-6(E)-heptenoate stereoisomers were prepared in enantiopure form starting from 10, utilizing selective reduction and oxidation methods.
