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207791-30-8

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  • 2,4-PYRROLIDINEDIONE, 5-(HYDROXYMETHYL)-3-[HYDROXY[(1R,2S,4AR,6S,8AS)-1,2,4A,5,6,7,8,8A-OCTAHYDRO-1,3,6-TRIMETHYL-2-(1E,3E)-1,3-PENTADIENYL-1-NAPHTHALENYL]METHYLENE]-1-METHYL-, (3E,5R)-

    Cas No: 207791-30-8

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  • 2,4-Pyrrolidinedione, 5-(hydroxymethyl)-3-[hydroxy[(1R,2S,4aR,6S,8aS)-1,2,4a,5,6,7,8,8a-octahydro-1,3,6-trimethyl-2-(1E,3E)-1,3-pentadienyl-1-naphthalenyl]methylene]-1-methyl-, (3E,5R)-

    Cas No: 207791-30-8

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207791-30-8 Usage

General Description

The chemical compound, "(2R)-5-hydroxy-2-(hydroxymethyl)-1-methyl-4-({(1R,2S,6S,8aS)-1,3,6-trimethyl-2-[(1E,3E)-penta-1,3-dien-1-yl]-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl}carbonyl)-1,2-dihydro-3H-pyrrol-3-one," is a complex organic molecule with a number of functional groups and stereocenters. It contains a hydroxy, hydroxymethyl, and methyl group, as well as a pyrrolone ring and a carbonyl group. The compound also features a penta-1,3-dien-1-yl side chain attached to a cyclohexane ring system. The stereochemistry of the molecule is specified by the (2R) and (1R,2S,6S,8aS) prefixes, indicating the arrangement of substituents around certain chiral centers. (2R)-5-hydroxy-2-(hydroxymethyl)-1-methyl-4-({(1R,2S,6S,8aS)-1,3,6-trimethyl-2-[(1E,3E)-penta-1,3-dien-1-yl]-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl}carbonyl)-1,2-dihydro-3H-pyrrol-3-one may have potential applications in pharmaceutical or chemical research due to its complex structure and potentially varied reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 207791-30-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,7,9 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 207791-30:
(8*2)+(7*0)+(6*7)+(5*7)+(4*9)+(3*1)+(2*3)+(1*0)=138
138 % 10 = 8
So 207791-30-8 is a valid CAS Registry Number.

207791-30-8SDS

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 (3E,5R)-3-[[(1R,2S,6S,8aS)-1,3,6-trimethyl-2-[(1E,3E)-penta-1,3-dienyl]-4a,5,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-hydroxymethylidene]-5-(hydroxymethyl)-1-methylpyrrolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 2,4-Pyrrolidinedione,5-(hydroxymethyl)-3-(hydroxy((1R,2S,4aR,6S,8aS)-1,2,4a,5,6,7,8,8a-octahydro-1,3,6-trimethyl-2-(1E,3E)-1,3-pentadienyl-1-naphthalenyl)methylene)-1-methyl-,(3E,5R)

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

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More Details:207791-30-8 SDS

207791-30-8Upstream product

207791-30-8Downstream Products

207791-30-8Relevant articles and documents

Equisetin and a novel opposite stereochemical homolog phomasetin, two fungal metabolites as inhibitors of HIV-1 integrase

Singh, Sheo B.,Zink, Deborah L.,Goetz, Michael A.,Dombrowski, Anne W.,Polishook, Jon D.,Hazuda, Daria J.

, p. 2243 - 2246 (1998)

Integration is an essential step in HIV replication and is catalyzed by an enzyme called integrase. We have isolated equisetin (1a), and a novel opposite stereochemical homolog, phomasetin (2a), from Fusarium heterosporum and a Phoma sp. respectively. They inhibit the invitro recombinant integrase enzyme with IC50 values of 7-20 μM. Unlike known inhibitors, these compounds also inhibit the integration reactions catalyzed by preintegration complexes isolated from HIV-1 infected cells.

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