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CAS

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70588-06-6

Chrysoobtusin, a flavonoid compound isolated from the leaves of the Chrysophyllum albidum plant, also known as the African star apple, exhibits a range of pharmacological properties. It is characterized by its antioxidant, anti-inflammatory, and anti-diabetic effects, which are attributed to its ability to inhibit enzymes associated with inflammation and oxidative stress, as well as its capacity to lower blood sugar levels in animal studies. These attributes position Chrysoobtusin as a promising candidate for therapeutic applications in managing diabetes and inflammation-related diseases, pending further research into its mechanisms of action and clinical potential.

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  • 70588-06-6 Structure

  • Basic information

    1. Product Name: Chrysoobtusin
    2. Synonyms: Chrysoobtusin;2-Hydroxy-1,6,7,8-tetramethoxy-3-methylanthraquinone;2-Hydroxy-1,6,7,8-tetramethoxy-3-methylanthracene-9,10-dione;2-Hydroxy-1,6,7,8-tetramethoxy-3-methyl-9,10-anthraquinone
    3. CAS NO:70588-06-6
    4. Molecular Formula: C19H18O7
    5. Molecular Weight: 358.34202
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 70588-06-6.mol

  • Chemical Properties

    1. Melting Point: 215-216℃
    2. Boiling Point: 586.2°C at 760 mmHg
    3. Flash Point: 212.4°C
    4. Appearance: /
    5. Density: 1.328±0.06 g/cm3 (20 ºC 760 Torr)
    6. Vapor Pressure: 2.44E-14mmHg at 25°C
    7. Refractive Index: 1.598
    8. Storage Temp.: 2-8°C(protect from light)
    9. Solubility: N/A
    10. CAS DataBase Reference: Chrysoobtusin(CAS DataBase Reference)
    11. NIST Chemistry Reference: Chrysoobtusin(70588-06-6)
    12. EPA Substance Registry System: Chrysoobtusin(70588-06-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 70588-06-6(Hazardous Substances Data)

70588-06-6 Usage

Uses

Used in Pharmaceutical Industry:
Chrysoobtusin is used as a potential therapeutic agent for the treatment of diabetes due to its demonstrated ability to reduce blood sugar levels in animal studies. Its anti-inflammatory properties also suggest its potential use in managing inflammation-related diseases.
Used in Nutraceutical Industry:
Given its antioxidant properties, Chrysoobtusin is used as a natural supplement to support overall health by combating oxidative stress, which is implicated in various chronic diseases.
Used in Research and Development:
Chrysoobtusin is utilized in scientific research as a subject for further exploration into its pharmacological mechanisms, potential synergistic effects with other compounds, and its safety and efficacy in clinical settings.

Check Digit Verification of cas no

The CAS Registry Mumber 70588-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,8 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70588-06:
(7*7)+(6*0)+(5*5)+(4*8)+(3*8)+(2*0)+(1*6)=136
136 % 10 = 6
So 70588-06-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H18O7/c1-8-6-9-12(18(25-4)14(8)20)16(22)13-10(15(9)21)7-11(23-2)17(24-3)19(13)26-5/h6-7,20H,1-5H3

70588-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Hydroxy-1,6,7,8-tetramethoxy-3-methylanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names Chryso-obtusin

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:70588-06-6 SDS

70588-06-6Downstream Products

70588-06-6Relevant articles and documents

SYNTHESIS OF SPECIFICALLY O-ALKYLATED ANTHRAQUINONES BY CYCLOADDITION

Cameron, Donald W.,Feutrill, Geoffrey I.,Gamble, Glenn B.,Stavrakis, John

, p. 4999 - 5002 (2007/10/02)

Cycloadducts from naphthoquinonoid dienophiles and 1-methoxy-1-trimethylsilyloxy butadienes undergo controlled aromatisation to form chiefly α-hydroxy- or α-methoxy-anthraquinones; this has led to synthesis of several natural O-methyl polyoxyanthraquinones.

Studies on the Constituents of the Seeds of Cassia obtusifolia LINN. The Structures of Two New Anthraquinone Glycosides

Kitanaka, Susumu,Kimura, Fumie,Takido, Michio

, p. 1274 - 1276 (2007/10/02)

Two new athraquinones, alaternin 1-O-β-D-glucopyranoside and chryso-obtusin 2-O-β-D-glucopyranoside, were isolated, along with physcion 8-O-β-D-glucopyranoside, from the seeds of Cassia obtusifolia LINN., and their structures were established on the basis of spectral and chemical evidence.Keywords - Cassia obtusifolia; Leguminosae; anthraquinone glucoside; physcion 8-O-β-D-glucopyranoside; alaternin 1-O-β-D-glucopyranoside; chryso-obtusin 1-O-β-D-glucopyranoside

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