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3-Hydroxy-2,8-dimethyl-1,4-phenanthrenedione, also known as 3-Hydroxy-2,8-dimethyl-1,4-naphthoquinone, is a naturally occurring organic compound with the molecular formula C16H12O3. It belongs to the class of phenanthrenes and derivatives, found in various plants such as Chrozophora tinctoria and Euclea undulata. 3-Hydroxy-2,8-dimethyl-1,4-phenanthrenedione is of interest in the field of natural product chemistry and medicinal research due to its potential biological activities, including antiviral, anti-tumor, antioxidant, and anti-inflammatory effects.

65907-77-9

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65907-77-9 Usage

Uses

Used in Pharmaceutical Synthesis:
3-Hydroxy-2,8-dimethyl-1,4-phenanthrenedione is used as an intermediate in the synthesis of pharmaceuticals for its potential therapeutic properties.
Used in Antiviral Applications:
In the field of virology, 3-Hydroxy-2,8-dimethyl-1,4-phenanthrenedione is used as an antiviral agent, leveraging its potential to inhibit viral replication and reduce the severity of viral infections.
Used in Anti-tumor Applications:
3-Hydroxy-2,8-dimethyl-1,4-phenanthrenedione is used as an anti-tumor agent, showing promise in the prevention and treatment of cancer due to its ability to interfere with tumor growth and proliferation.
Used in Antioxidant Formulations:
3-Hydroxy-2,8-dimethyl-1,4-phenanthrenedione is used as an antioxidant in various formulations to protect cells from oxidative damage, which is implicated in many diseases and aging processes.
Used in Anti-inflammatory Formulations:
3-Hydroxy-2,8-dimethyl-1,4-phenanthrenedione is used as an anti-inflammatory agent to reduce inflammation and associated pain, which is beneficial in treating various inflammatory conditions.
Used in Natural Product Chemistry Research:
In academic and industrial research, 3-Hydroxy-2,8-dimethyl-1,4-phenanthrenedione is used as a subject of study for understanding its structure-activity relationships and exploring its potential applications in drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 65907-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,0 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65907-77:
(7*6)+(6*5)+(5*9)+(4*0)+(3*7)+(2*7)+(1*7)=159
159 % 10 = 9
So 65907-77-9 is a valid CAS Registry Number.

65907-77-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name danshenxinkun C

1.2 Other means of identification

Product number -
Other names danshexinkun C

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:65907-77-9 SDS

65907-77-9Downstream Products

65907-77-9Relevant academic research and scientific papers

Ultrasound-promoted synthesis of substituted phenanthrene-1,4-quinones; the structure of plectranthon D

Zhang, Zhao-Rong,Flachsmann, Felix,Moghaddam, Firouz Matloubi,Rueedi, Peter

, p. 2153 - 2156 (2007/10/02)

A series of tanshinone-type diterpenoids was prepared by ultrasound-promoted and Lewis acid catalyzed, highly regioselective cycloadditions of styrenes with substituted 1,4-benzoquinones as the key step.

TOTAL SYNTHESIS OF DAN SHEN DITERPENOID QUINONES

Danheiser, Rick L.,Casebier, David S.,Loebach, Jennifer L.

, p. 1149 - 1152 (2007/10/02)

A photochemical aromatic annulation strategy provides efficient synthetic routes to the diterpenoid quinones (+)-danshexinkun A, danshexinkun B, danshexinkun C, (-)-dihydrotanshinone I, and tanshinone I.

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