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917805-74-4

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  • Factory Supply tert.butyl amine salt of (+)-(3R, 5S)-7[4-(4-Fluorophenyl)-6-Isopropyl-2 [methyl-(methylsulfonyl amino] pyrimidin-5-yl]-3,5- dihydroxy-6(E)- heptenoic acid

    Cas No: 917805-74-4

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  • (3R,5S,6E)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-(propan-2-yl)pyrimidin-5-yl]-3,5-dihydroxyhept-6-enoic acid-2-methylpropan-2-amine

    Cas No: 917805-74-4

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917805-74-4 Usage

Description

(3R,5S,6E)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-(propan-2-yl)pyrimidin-5-yl]-3,5-dihydroxyhept-6-enoic acid-2-methylpropan-2-amine is a complex organic molecule characterized by the presence of a pyrimidine ring, a fluorophenyl group, a methylsulfonyl group, and a 3,5-dihydroxyhept-6-enoic acid chain. Additionally, it features a 2-methylpropan-2-amine side chain. (3R,5S,6E)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-(propan-2-yl)pyrimidin-5-yl]-3,5-dihydroxyhept-6-enoic acid-2-methylpropan-2-amine's multiple functional groups and stereochemistry contribute to its intricate structure, making it a challenging molecule to synthesize and study. Due to its unique features, it may possess potential biological activity and could be explored for applications in pharmaceutical research or drug development.

Uses

Used in Pharmaceutical Research:
(3R,5S,6E)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-(propan-2-yl)pyrimidin-5-yl]-3,5-dihydroxyhept-6-enoic acid-2-methylpropan-2-amine is used as a compound of interest in pharmaceutical research for its potential biological activity. The presence of various functional groups and its complex structure suggest that it may interact with biological targets in ways that could lead to the development of new therapeutic agents.
Used in Drug Development:
In the field of drug development, (3R,5S,6E)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-(propan-2-yl)pyrimidin-5-yl]-3,5-dihydroxyhept-6-enoic acid-2-methylpropan-2-amine may be utilized as a lead compound. Its unique structural features could be optimized to enhance its pharmacological properties, such as potency, selectivity, and bioavailability, making it a candidate for further investigation and potential clinical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 917805-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,8,0 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 917805-74:
(8*9)+(7*1)+(6*7)+(5*8)+(4*0)+(3*5)+(2*7)+(1*4)=194
194 % 10 = 4
So 917805-74-4 is a valid CAS Registry Number.

917805-74-4Downstream Products

917805-74-4Relevant articles and documents

Method for the preparation of high purity Rosuvastatin Calcium salt

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, (2017/01/17)

The present invention relates to a method for manufacturing a Rosuvastatin calcium salt by using a Rosuvastatin tert-butyl amine salt, and to a method for manufacturing a high purity Rosuvastatin calcium salt, which has impurities less than 0.1% of a diastereomer. The manufacturing method of a high purity Rosuvastatin calcium salt comprises the steps of: 1) manufacturing a compound represented by chemical formula III by reducing a compound represented by chemical formula IV; 2) manufacturing a compound represented by chemical formula II by adding t-butyl amine; and 3) manufacturing a compound represented by chemical formula I by adding a calcium ion to the compound represented by chemical formula II.COPYRIGHT KIPO 2016

AMINE SALTS OF PITAVASTATIN AND ROSUVASTATIN

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Page/Page column 16; 17, (2014/10/15)

The present invention relates to oxygen-comprising amine salts of HMG-CoA reductase inhibitors, to a method of producing said amine salts and to the use of said amine salts in the production of pharmaceutically acceptable salts of HMG-CoA reductase inhibi

NOVEL INTERMEDIATES FOR THE PREPARATION OF HMG-CoA REDUCTASE INHIBITORS

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, (2013/06/27)

The present invention provides a process for preparing novel intermediates of Formula wherein, R1 can be hydrogen, C1-C4 alkyl, halogen, nitro, hydroxy, or C1-C4 alkoxy; Rx can be selected from hydrophobic residue of HMG-CoA reductase inhibitors; which can be effectively used for the preparation of HMG-CoA reductase inhibitors such as rosuvastatin and pharmaceutically acceptable salts thereof.

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