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146905-24-0

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146905-24-0 Usage

General Description

1,2-Diacetoxy-4,7,8-trihydroxy-3-(4-hydroxyphenyl)dibenzofuran is a complex chemical compound that contains acetoxy and hydroxy functional groups as well as a dibenzofuran backbone. It is also known as DAF-22 and is a natural product that has been isolated from the fungus Dichomitus squalens. This chemical has been found to exhibit potent antioxidant and radical scavenging properties, making it potentially useful in various pharmaceutical and medicinal applications. However, further research is needed to fully understand its potential therapeutic uses and any potential side effects or toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 146905-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,9,0 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 146905-24:
(8*1)+(7*4)+(6*6)+(5*9)+(4*0)+(3*5)+(2*2)+(1*4)=140
140 % 10 = 0
So 146905-24-0 is a valid CAS Registry Number.

146905-24-0SDS

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 4,7,8-Trihydroxy-3-(4-hydroxyphenyl)dibenzo[b,d]furan-1,2-diyl di acetate

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:146905-24-0 SDS

146905-24-0Relevant articles and documents

Syntheses of the fungal metabolites Boletopsins 7, 11, and 12 from the Papua New Guinea medicinal mushroom Boletopsis sp.

Beekman, Andrew M.,Barrow, Russell A.

, p. 1017 - 1024 (2014/03/21)

Boletopsins 7 (1), 11 (2), and 12 (3) are p-terphenyl dibenzofuran compounds, isolated from the Papua New Guinean medicinal mushroom Boletopsis sp. The first syntheses of these fungal metabolites are reported, allowing for an investigation of their antibiotic activity. The key steps include sequential Suzuki-Miyaura couplings to rapidly form the p-terphenyl backbone and an Ullmann ether synthesis on a formate ester to create the dibenzofuran moiety. Biological evaluation of the synthetic compounds and intermediates against a panel of bacterial nosocomial pathogens was performed.

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