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2,5-Bis(benzoyloxy)-3,6-bis(4-hydroxyphenyl)-2,5-cyclohexadiene-1,4-dione is a complex organic compound with the molecular formula C28H18O8. It is a derivative of cyclohexadiene-1,4-dione, featuring two benzoyloxy groups at the 2 and 5 positions, and two 4-hydroxyphenyl groups at the 3 and 6 positions. 2,5-Bis(benzoyloxy)-3,6-bis(4-hydroxyphenyl)-2,5-cyclohexadiene-1,4-dione is known for its potential applications in the synthesis of various organic compounds and materials, particularly in the field of polymer chemistry. Its structure provides a rigid backbone with multiple functional groups, which can be further modified or used as a building block for more complex molecules. The compound's properties, such as its reactivity and stability, make it a valuable intermediate in the development of new materials with specific characteristics.

548-32-3

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548-32-3 Usage

Type of compound

Organic compound

Derivative

Benzoic acid

Functional groups

Two benzoyl groups, two hydroxyphenyl groups

Chemical structure

Cyclohexadiene-1,4-dione backbone

Applications

Acne treatment products, bleaching agent for flour, production of polymer resins, radical initiator in chemical reactions

Properties

Antimicrobial, effective in treating acne by reducing bacteria and inflammation

Side effects

Skin irritation and dryness in some individuals

Check Digit Verification of cas no

The CAS Registry Mumber 548-32-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 548-32:
(5*5)+(4*4)+(3*8)+(2*3)+(1*2)=73
73 % 10 = 3
So 548-32-3 is a valid CAS Registry Number.
InChI:InChI=1/C32H20O8/c33-23-15-11-19(12-16-23)25-28(36)30(40-32(38)22-9-5-2-6-10-22)26(20-13-17-24(34)18-14-20)27(35)29(25)39-31(37)21-7-3-1-4-8-21/h1-18,33-34H

548-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-benzoyloxy-2,5-bis(4-hydroxyphenyl)-3,6-dioxocyclohexa-1,4-dien-1-yl] benzoate

1.2 Other means of identification

Product number -
Other names 2,5-bis-benzoyloxy-3,6-bis-(4-hydroxy-phenyl)-[1,4]benzoquinone

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:548-32-3 SDS

548-32-3Downstream Products

548-32-3Relevant academic research and scientific papers

Thelephantins I-N: p-terphenyl derivatives from the inedible mushroom Hydnellum caeruleum

Quang, Dang Ngoc,Hashimoto, Toshihiro,Hitaka, Yuki,Tanaka, Masami,Nukada, Makiko,Yamamoto, Isao,Asakawa, Yoshinori

, p. 1179 - 1184 (2004)

Phytochemical investigation of the methanolic extract of the fruiting bodies of the inedible mushroom Hydnellum caeruleum resulted in the isolation of six p-terphenyl derivatives named thelephantins I-N (1-6), together with a known compound, dihydroaurantiacin dibenzoate (7). These structures were determined by high-resolution MS, 2D NMR, IR and UV spectroscopic analysis, and by the chemical reactions.

Fungal Pigments, 61. - Flavomentins and Spiromentins, Novel Terphenylquinone Derivatives from Paxillus atrotomentosus and P. panuoides (Boletales)

Besl, Helmut,Bresinsky, Andreas,Geigenmueller, Georg,Herrmann, Rupert,Kilpert, Claus,Steglich, Wolfgang

, p. 803 - 810 (2007/10/02)

The gilled toadstools Paxillus atrotomentosus and P. panuoides produce small amounts of orange-yellow flavomentins and violet spiromentins.The flavomentins 1-3 constitute mono- and diesters of atromentin (6) with (2Z,4E)-2,4-hexadienoic acid or (2Z,4S,5S)

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