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129332-29-2

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  • High quality T-Butyl(E)-3,5-Dihydroxy-7-[3'-(4''-Fluorophenyl)-1'-Methylethyl-Indol-2'-Yl]-6-Heptenoate supplier in China

    Cas No: 129332-29-2

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  • Simagchem Corporation
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  • Factory Price API 99% tert-Butyl (E)-3,5-dihydroxy-7-[3'-(4''-fluorophenyl)-1'-methylethyl-indol-2'-yl]-6-heptenoate 129332-29-2 GMP Manufacturer

    Cas No: 129332-29-2

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  • Xi'an Xszo Chem Co., Ltd.
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  • tert-Butyl (E)-3,5-dihydroxy-7-[3'-(4"-fluorophenyl)-1'-methylethyl-indol-2'-yl]-6-heptenoate

    Cas No: 129332-29-2

  • USD $ 1.2-5.0 / Kiloliter

  • 5 Kiloliter

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  • Chemwill Asia Co., Ltd.
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  • 6-Heptenoic acid,7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-3,5-dihydroxy-,1,1-dimethylethyl ester, (3R,5S,6E)-rel- 129332-29-2

    Cas No: 129332-29-2

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  • Shanghai Upbio Tech Co.,Ltd
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129332-29-2 Usage

Description

tert-Butyl (E)-3,5-dihydroxy-7-[3'-(4''-fluorophenyl)-1'-methylethyl-indol-2'-yl]-6-heptenoate is a complex organic compound with a unique molecular structure. It is characterized by the presence of a tert-butyl group, two hydroxyl groups, and a heptenoate chain. The molecule also features a 3'-(4''-fluorophenyl)-1'-methylethyl-indol-2'-yl moiety, which contributes to its distinct properties and potential applications.

Uses

Used in Pharmaceutical Industry:
tert-Butyl (E)-3,5-dihydroxy-7-[3'-(4''-fluorophenyl)-1'-methylethyl-indol-2'-yl]-6-heptenoate is used as a synthetic HMG-CoA reductase inhibitor for antilipemic purposes. It helps in reducing the levels of low-density lipoprotein (LDL) cholesterol and triglycerides in the blood, thus playing a crucial role in the management of hyperlipidemia and cardiovascular diseases.
Used in Drug Synthesis:
Due to its unique molecular structure, tert-Butyl (E)-3,5-dihydroxy-7-[3'-(4''-fluorophenyl)-1'-methylethyl-indol-2'-yl]-6-heptenoate can be used as a key intermediate in the synthesis of various pharmaceutical compounds. Its presence of functional groups such as hydroxyl and heptenoate chain allows for further chemical modifications and the development of new drugs with improved therapeutic properties.
Used in Research and Development:
tert-Butyl (E)-3,5-dihydroxy-7-[3'-(4''-fluorophenyl)-1'-methylethyl-indol-2'-yl]-6-heptenoate can also be utilized in research and development settings to study its potential applications in various fields, such as drug discovery, medicinal chemistry, and biochemistry. Researchers can explore its interactions with biological targets, evaluate its pharmacological properties, and investigate its potential as a lead compound for the development of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 129332-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,3,3 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129332-29:
(8*1)+(7*2)+(6*9)+(5*3)+(4*3)+(3*2)+(2*2)+(1*9)=122
122 % 10 = 2
So 129332-29-2 is a valid CAS Registry Number.

129332-29-2 Well-known Company Product Price

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  • (1285964)  Fluvastatin Related Compound B  United States Pharmacopeia (USP) Reference Standard

  • 129332-29-2

  • 1285964-15MG

  • 14,578.20CNY

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129332-29-2SDS

SAFETY DATA SHEETS

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.Identification

1.1 GHS Product identifier

Product name tert-Butyl (E)-3,5-dihydroxy-7-[3'-(4''-fluorophenyl)-1'-methylethyl-indol-2'-yl]-6-heptenoate

1.2 Other means of identification

Product number -
Other names Fluvastatin Related Compound B

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:129332-29-2 SDS

129332-29-2Downstream Products

129332-29-2Relevant articles and documents

PROCESS FOR THE PREPARATION OF FLUVASTATIN AND SALTS THEREOF

-

, (2012/02/15)

The present invention relates to an improved process for the preparation of fluvastatin or pharmaceutical acceptable salts or derivatives thereof, in particular to a one-pot process for large scale production of Fluvastatin and salts thereof in high yield

An Improved Manufacturing Process for Fluvastatin

Fuenfschilling, Peter C.,Hoehn, Pascale,Mutz, Jean-Paul

, p. 13 - 18 (2012/12/26)

An improved manufacturing process for fluvastatin 1 has been developed by performing the condensation reaction of E-[3-(4fluorophenyl)-l-(l-methylethyl)- lH-indol-2-yl]-2-propenal, 4, with the dianion of tert-butyl acetoacetate and the subsequent low-temp

PROCESS FOR THE PREPARATION OF INDOLE DERIVATIVES BY ENZYMATIC ACYLATION

-

Page 18-19, (2008/06/13)

A process for the preparation of compounds of formula (1), by enzymatic acylation to form compounds of formulae (3a) and (3a') and then reacting the compound of formula (3a) with a compound introducing the radical of formula -CH2-COOR8

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