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3,4-Dihydro-3,6,9-trihydroxy-7-methoxy-3-methyl-1H-naphtho[2,3-c]pyran-5,10-dione is a complex organic molecule characterized by a naphtho[2,3-c]pyran core structure. It features three hydroxyl groups, a methoxy group, and a methyl substituent, classifying it as a naphthoquinone derivative. 3,4-Dihydro-3,6,9-trihydroxy-7-methoxy-3-methyl-1H-naphtho[2,3-c]pyran-5,10-dione is notable for its antioxidant and antitumor properties, which have been the subject of research for potential medicinal applications, particularly in anti-inflammatory and anticancer activities. Its unique structure and bioactivity make 3,4-Dihydro-3,6,9-trihydroxy-7-methoxy-3-methyl-1H-naphtho[2,3-c]pyran-5,10-dione a promising candidate for further exploration in pharmaceuticals and natural product chemistry.

1702-77-8

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1702-77-8 Usage

Uses

Used in Pharmaceutical Industry:
3,4-Dihydro-3,6,9-trihydroxy-7-methoxy-3-methyl-1H-naphtho[2,3-c]pyran-5,10-dione is used as a potential therapeutic agent for its antioxidant properties, which may contribute to the prevention or treatment of various diseases associated with oxidative stress.
Used in Anticancer Applications:
In the field of oncology, 3,4-Dihydro-3,6,9-trihydroxy-7-methoxy-3-methyl-1H-naphtho[2,3-c]pyran-5,10-dione is utilized as an anticancer agent due to its ability to target and inhibit the growth of cancer cells. Its antitumor activity is of interest for the development of novel cancer treatments.
Used in Anti-inflammatory Applications:
3,4-Dihydro-3,6,9-trihydroxy-7-methoxy-3-methyl-1H-naphtho[2,3-c]pyran-5,10-dione is employed as an anti-inflammatory agent, leveraging its capacity to reduce inflammation, which is beneficial in managing conditions characterized by excessive immune responses.
Used in Natural Product Chemistry:
In the realm of natural product chemistry, 3,4-Dihydro-3,6,9-trihydroxy-7-methoxy-3-methyl-1H-naphtho[2,3-c]pyran-5,10-dione serves as a subject of study for understanding its structure-activity relationships, potentially leading to the discovery of new bioactive compounds with improved pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1702-77-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,0 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1702-77:
(6*1)+(5*7)+(4*0)+(3*2)+(2*7)+(1*7)=68
68 % 10 = 8
So 1702-77-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O7/c1-15(20)4-6-7(5-22-15)13(18)10-8(16)3-9(21-2)14(19)11(10)12(6)17/h3,17-18,20H,4-5H2,1-2H3

1702-77-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5,10-trihydroxy-7-methoxy-3-methyl-1,4-dihydrobenzo[g]isochromene-6,9-dione

1.2 Other means of identification

Product number -
Other names Fusarubin

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:1702-77-8 SDS

1702-77-8Upstream product

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