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  • 6-Heptenoic acid,7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-5-hydroxy-3-oxo-,1,1-dimethylethyl ester, (5S,6E)- 194934-95-7

    Cas No: 194934-95-7

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  • 1 Kilogram

  • 10000 Metric Ton/Month

  • Shanghai Upbio Tech Co.,Ltd
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  • tert-Butyl (E)-7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-5-hydroxy-3-oxo-6-heptenoate

    Cas No: 194934-95-7

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  • 1 Kilogram

  • 1-100 Kilogram/Month

  • Afine Chemicals Limited
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194934-95-7 Usage


tert-Butyl (E)-7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-5-hydroxy-3-oxo-6-heptenoate is a complex organic compound with a molecular structure that features a fluorophenyl group, an indole ring, and a t-butyl ester group. It is characterized by its (E)-configuration, which refers to the geometry of the double bond in the molecule. tert-Butyl (E)-7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-5-hydroxy-3-oxo-6-heptenoate is likely to have specific applications in the pharmaceutical or chemical industries due to its unique structure and functional groups.


Used in Pharmaceutical Industry:
tert-Butyl (E)-7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-5-hydroxy-3-oxo-6-heptenoate is used as a reactant in the synthesis of various pharmaceutical compounds. Its unique molecular structure, including the fluorophenyl and indole moieties, may contribute to the development of new drugs with specific therapeutic properties.
Used in Chemical Synthesis:
In the chemical industry, tert-Butyl (E)-7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-5-hydroxy-3-oxo-6-heptenoate can be used as an intermediate in the synthesis of other complex organic molecules. Its functional groups, such as the ester and hydroxyl groups, can be further modified to produce a variety of compounds with different applications.
Used in Research and Development:
Due to its unique structure, tert-Butyl (E)-7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-5-hydroxy-3-oxo-6-heptenoate may also be utilized in research and development for studying the properties and reactivity of similar compounds. It can serve as a model compound for understanding the behavior of related molecules in various chemical reactions and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 194934-95-7 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 194934-95:
187 % 10 = 7
So 194934-95-7 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 tert-Butyl (E)-7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-5-hydroxy-3-oxo-6-heptenoate

1.2 Other means of identification

Product number -
Other names Fluvastatin tert-butyl ester

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:194934-95-7 SDS

194934-95-7Relevant 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 (1997)

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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