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Dihydromevinolin, also known as 4a,5-Dihydro Lovastatin, is an impurity found in Lovastatin bulk drug. It is a chemical compound that is produced during the manufacturing process of Lovastatin, a widely used cholesterol-lowering medication.

77517-29-4

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77517-29-4 Usage

Uses

Dihydromevinolin is used as an impurity in the production of Lovastatin bulk drug. It is important to monitor and control the levels of this impurity to ensure the safety and efficacy of the final product. The presence of dihydromevinolin can affect the quality and performance of Lovastatin, so it is crucial to minimize its concentration during the manufacturing process.

Check Digit Verification of cas no

The CAS Registry Mumber 77517-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,1 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77517-29:
(7*7)+(6*7)+(5*5)+(4*1)+(3*7)+(2*2)+(1*9)=154
154 % 10 = 4
So 77517-29-4 is a valid CAS Registry Number.
InChI:InChI=1/C24H38O5/c1-5-15(3)24(27)29-21-11-14(2)10-17-7-6-16(4)20(23(17)21)9-8-19-12-18(25)13-22(26)28-19/h6-7,14-21,23,25H,5,8-13H2,1-4H3/t14-,15-,16-,17-,18+,19+,20-,21-,23+/m0/s1

77517-29-4 Well-known Company Product Price

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  • USP

  • (1370611)  Lovastatin Related Compound A  United States Pharmacopeia (USP) Reference Standard

  • 77517-29-4

  • 1370611-20MG

  • 15,221.70CNY

  • Detail

77517-29-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,3S,4aR,7S,8S,8aR)-8-{2-[(2R,4R)-4-Hydroxy-6-oxotetrahydro-2H- pyran-2-yl]ethyl}-3,7-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naph thalenyl (2S)-2-methylbutanoate

1.2 Other means of identification

Product number -
Other names -

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:77517-29-4 SDS

77517-29-4Upstream product

77517-29-4Downstream Products

77517-29-4Relevant articles and documents

Total Synthesis of (+)-Dihydromevinolin

Hecker, Scott J.,Heathcock, Clayton H.

, p. 4586 - 4594 (2007/10/02)

A total syntheses of (+)-dihydromevinolin (2b) is presented, as well as the preparation of three analogues (62, 63, and 64) for assessment of their biological activity.Base-promoted fragmentation of the tosylhydrazone (20) of key intermediate 6 affords ac

Reductive Transformation and Cyclopropanation of Mevinolin (α-Methylcompactin). Generation of Chirality in the 1,4-Hydrostannation of a Cyclic Diene

Kuo, C. H.,Patchett, A. A.,Wendler, N. L.

, p. 1991 - 1998 (2007/10/02)

Conversion of mevinolin by direct reductive procedures as well as by indirect chemical transformations has permitted the preparation of the various di- and tetrahydro derivatives.Cyclopropanation of mevinolin and its derivatives has furnished mono- and di

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