2-bromo-1,4-dihydroxyanthraquinone

Chinese Factory Supply Wholesale 2-bromo-1,4-dihydroxyanthraquinone 81-52-7 with Cheap Price We supply high quality 2-bromo-1,4-dihydroxyanthraquinone (CAS 81-52-7), in stock, factory directly supply to clients, lower prices, more competitiveness.

What is the 2-bromo-1,4-dihydroxyanthraquinone ?

2-bromo-1,4-dihydroxyanthraquinone is , while it's Molecular Formula is C14H7BrO4.

What is the CAS number for 2-bromo-1,4-dihydroxyanthraquinone ?

The CAS number of 2-bromo-1,4-dihydroxyanthraquinone is 81-52-7.

More information of 2-bromo-1,4-dihydroxyanthraquinone 81-52-7 are:

Synonyms	Anthraquinone,2-bromo-1,4-dihydroxy- (6CI,8CI);1,4-Dihydroxy-2-bromoanthraquinone;2-Bromo-1,4-dihydroxyanthraquinone;2-Bromoquinizarin;2-Bromo-1,4-dihydroxyanthracene-9,10-dione;2-Bromo-1,4-dihydroxy-9,10-anthraquinone;
CAS?Number	81-52-7
Molecular Formula	C14H7BrO4
Molecular Weight	319.111
Density	1.854 g/cm³
Boiling Point	484.4 °C at 760 mmHg
Flash Point	246.7 °C
PSA	74.60000
LogP	2.63570

What is 2-bromo-1,4-dihydroxyanthraquinone (81-52-7) used for?

2-bromo-1,4-dihydroxyanthraquinone is a chemical compound with the molecular formula C14H7BrO4. It is a derivative of anthraquinone, a type of organic compound with a fused four-ring structure. The presence of a bromine atom at the 2-position and hydroxyl groups at the 1 and 4 positions gives 2-bromo-1,4-dihydroxyanthraquinone unique properties. It is often used as an intermediate in the synthesis of dyes and pigments due to its ability to form various colored compounds. The compound is also known for its potential applications in the pharmaceutical industry and as a chemical reagent. Its chemical structure and functional groups make it a versatile building block in organic synthesis, particularly in the preparation of complex molecules with specific color properties or therapeutic effects.

InChI:InChI=1/C14H7BrO4/c15-8-5-9(16)10-11(14(8)19)13(18)7-4-2-1-3-6(7)12(10)17/h1-5,16,19H

Articles related to 2-bromo-1,4-dihydroxyanthraquinone:

Article

Source

An investigation of the reaction mechanism of the bis-acylation of aromatics with o-phthaloyl dichlorides: Regioselective synthesis of anthraquinones

Sartori,Bigi,Tao,Porta,Maggi,Predieri,Lanfranchi,Pellinghelli

, p. 6588 - 6591 (2007/10/03)

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