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70588-06-6

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70588-06-6 Usage

General Description

Chrysoobtusin is a chemical compound extracted from the leaves of the Chrysophyllum albidum plant, also known as the African star apple. It is a flavonoid with potential pharmacological properties, including antioxidant, anti-inflammatory, and anti-diabetic effects. Chrysoobtusin has been found to inhibit the activity of enzymes involved in inflammation and oxidative stress, as well as demonstrate the ability to reduce blood sugar levels in animal studies. These findings suggest that Chrysoobtusin may have potential therapeutic applications in the treatment of conditions such as diabetes and inflammation-related diseases. Further research is needed to fully understand the mechanisms of action and potential clinical uses of Chrysoobtusin.

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.

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