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901765-36-4

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  • (S,E)-ETHYL 7-(4-(4-FLUOROPHENYL)-6-ISOPROPYL-2-(N-METHYLMETHYLSULFONAMIDO)PYRIMIDIN-5-YL)-5-HYDROXY-3-OXOHEPT-6-ENOATE

    Cas No: 901765-36-4

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  • 901765-36-4 (S,E)-Ethyl 7-(4-(4-fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)-5-hydroxy-3-oxohept-6-enoate

    Cas No: 901765-36-4

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  • 6-Heptenoic Acid,7-[4-(4-Fluorophenyl)-6-(1-Methylethyl)-2-[Methyl(Methylsulfonyl)Amino]-5-Pyrimidinyl]-5-Hydroxy-3-Oxo-, Ethyl Ester, (5S,6E)-

    Cas No: 901765-36-4

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  • (5S,6E)-7-[4-(4-Fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]-5-hydroxy-3-oxo-6-heptenoic acid ethyl ester

    Cas No: 901765-36-4

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901765-36-4 Usage

Uses

901765-36-4 is a reagent in production of rosuvastatin.

Check Digit Verification of cas no

The CAS Registry Mumber 901765-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,1,7,6 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 901765-36:
(8*9)+(7*0)+(6*1)+(5*7)+(4*6)+(3*5)+(2*3)+(1*6)=164
164 % 10 = 4
So 901765-36-4 is a valid CAS Registry Number.

901765-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (5S)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-propan-2-ylpyrimidin-5-yl]-5-hydroxy-3-oxohept-6-enoate

1.2 Other means of identification

Product number -
Other names 3-keto-5-hydroxy-ethyl rosuvastatin

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:901765-36-4 SDS

901765-36-4Relevant articles and documents

Efficient and highly stereoselective assembly of rosuvastatin

?terk, Damjan,Zaugg, Werner,Beutler, Ulrich,Loeser, Eric M.,Prasad, Kapa,?asar, Zdenko

supporting information, p. 1338 - 1341 (2018/03/29)

We report an asymmetric synthesis of rosuvastatin starting from an α,β-unsaturated aldehyde precursor containing the rosuvastatin heterocyclic core at its terminus. The α,β-unsaturated carbonyl starting material was used in a highly stereoselective Ti-catalyzed aldol condensation followed by a syn-selective Narasaka–Prasad borane-ketone reduction and hydrolysis step to provide rosuvastatin calcium. This approach provides concise access to stereochemically pure rosuvastatin from simple and readily available starting materials in 3 steps. The overall three-step process provides rosuvastatin calcium in 80% yield, >99:1 syn/anti ratio, and >99% ee.

AN IMPROVED PROCESS FOR PREPARATION OF ROSUVASTATIN CALCIUM

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Page/Page column 21-24, (2008/12/08)

The present invention relates to an improved process for preparing (E)-7-[4-(4-fluorophenyl)- 6-isopropyl-2-[methyl(methylsulfonyl)amino]pyrimidin-5-yl](3R,5S)-3,5-dihydroxyhept-6- enoic acid calcium of Formula (I).

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