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(aR)-5,5',6,6',8,8'-Hexahydroxy-2,2'-dimethyl-9,9'-bi[4H-naphtho[2,3-b]pyran]-4,4'-dione is a complex organic compound with a molecular formula of C28H22O12. It is a derivative of the naturally occurring compound ellagic acid, which is found in various fruits and plants. This specific compound is characterized by its hexahydroxy (six hydroxyl groups) and dimethyl (two methyl groups) structure, as well as its bi[4H-naphtho[2,3-b]pyran]-4,4'-dione backbone. The compound exhibits various biological activities, such as antioxidant, anti-inflammatory, and anticancer properties, making it a potential candidate for pharmaceutical applications. Its chemical structure and properties make it an interesting subject for further research in the field of natural products chemistry and drug development.

3692-07-7

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3692-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3692-07-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,9 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3692-07:
(6*3)+(5*6)+(4*9)+(3*2)+(2*0)+(1*7)=97
97 % 10 = 7
So 3692-07-7 is a valid CAS Registry Number.

3692-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,8-trihydroxy-2-methyl-9-(5,6,8-trihydroxy-2-methyl-4-oxobenzo[g]chromen-9-yl)benzo[g]chromen-4-one

1.2 Other means of identification

Product number -
Other names Ustilaginoidin A

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:3692-07-7 SDS

3692-07-7Downstream Products

3692-07-7Relevant academic research and scientific papers

Enantioselective Phenol Coupling by Laccases in the Biosynthesis of Fungal Dimeric Naphthopyrones

Obermaier, Sebastian,Thiele, Wiebke,Fürtges, Leon,Müller, Michael

, p. 9125 - 9128 (2019/06/13)

Biaryl compounds are ubiquitous metabolites that are often formed by dimerization through oxidative phenol coupling. Hindered rotation around the biaryl bond can cause axial chirality. In nature, dimerizations are catalyzed by oxidative enzymes such as la

Methods of inhibiting phosphatase activity and treatment of disorders associated therewith using naphthopyrones and derivatives thereof

-

, (2008/06/13)

The present invention relates to organic molecules capable of inhibiting protein tyrosine phosphatase activity. The invention further relates to the use of such molecules to modulate or regulate signal transduction by inhibiting protein tyrosine phosphatase activity. Finally, the invention relates to the use of such molecules to treat various disease states including diabetes mellitus.

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