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  • (3R,5S,6E)-7-[3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-3,5-dihydroxy-6-heptenoic acid-1,1-dimethylethyl ester

    Cas No: 194934-96-8

  • USD $ 1.2-5.0 / Kiloliter

  • 5 Kiloliter

  • 3000 Metric Ton/Month

  • Chemwill Asia Co., Ltd.
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194934-96-8 Usage


tert-Butyl (E)-3,5-Dihydroxy-7-[3'-(4"-fluorophenyl)-1'-methylethylindol-2'-yl)hept-6-enoate is a complex organic compound characterized by its fluorophenyl and indole moieties. It is a derivative of hept-6-enoate with a tert-butyl group and two hydroxyl groups in the 3 and 5 positions, respectively. The compound exhibits an (E)-configuration, indicating the geometry of the double bond present in its structure.


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:
188 % 10 = 8
So 194934-96-8 is a valid CAS Registry Number.



According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017


1.1 GHS Product identifier

Product name (3R,5S)-Fluvastatin tert-Butyl Ester

1.2 Other means of identification

Product number -
Other names tert-Butyl (E)-3,5-Dihydroxy-7-[3'-(4"-fluorophenyl)-1'-methylethylindol-2'-yl)hept-6-enoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:194934-96-8 SDS

194934-96-8Relevant articles and documents

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.

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