1,3-DIBROMO-2,5-DIHYDROXYBENZENE

  • Name: 1,3-DIBROMO-2,5-DIHYDROXYBENZENE
  • CAS: 3333-25-3
  • Purity: 99%
Inquiry

Details

Manufacturer supply 1,3-DIBROMO-2,5-DIHYDROXYBENZENE 3333-25-3 with sufficient stock and high standard

  • Molecular Formula: C6H4 Br2 O2
  • Molecular Weight: 267.905
  • Vapor Pressure: 0.0019mmHg at 25°C 
  • Melting Point: 163-164 °C 
  • Boiling Point: 283°Cat760mmHg 
  • PKA: 7.62±0.23(Predicted) 
  • Flash Point: 124.9°C 
  • PSA： 40.46000 
  • Density: 2.257g/cm3 
  • LogP: 2.62280 

1,3-DIBROMO-2,5-DIHYDROXYBENZENE(Cas 3333-25-3) Usage

General Description

1,3-Dibromo-2,5-dihydroxybenzene is a chemical compound with the molecular formula C6H4Br2O2. It is a derivative of benzene and belongs to the class of organic compounds known as dibenzo-para-dioxins. 1,3-DIBROMO-2,5-DIHYDROXYBENZENE is used in organic synthesis and as a building block for the preparation of various other compounds. It is also used as a reagent in the production of pharmaceuticals and agrochemicals. Additionally, it has been studied for its potential biological and medicinal properties, particularly as an anti-inflammatory and antioxidant agent. However, it is important to handle this compound with caution, as it is considered to be toxic and harmful if ingested or inhaled.

InChI:InChI=1/C6H4Br2O2/c7-4-1-3(9)2-5(8)6(4)10/h1-2,9-10H

3333-25-3 Relevant articles

Peptide-Catalyzed Fragment Couplings that Form Axially Chiral Non-C2-Symmetric Biaryls

Coombs, Gavin,Sak, Marcus H.,Miller, Scott J.

supporting information, p. 2875 - 2880 (2020/01/24)

We have demonstrated that small, modular...

Novel bioactivation pathway of benzbromarone mediated by cytochrome P450

Kitagawara, Yumina,Ohe, Tomoyuki,Tachibana, Kumiko,Takahashi, Kyoko,Nakamura, Shigeo,Mashino, Tadahiko

supporting information, p. 1303 - 1306 (2015/09/07)

Benzbromarone (BBR) is a hepatotoxic dru...

Substrate specificity of Sphingobium chlorophenolicum 2,6- dichlorohydroquinone 1,2-dioxygenase

MacHonkin, Timothy E.,Doerner, Amy E.

body text, p. 8899 - 8913 (2012/05/05)

PcpA is an aromatic ring-cleaving dioxyg...

Benzopyrans as selective estrogen receptor β agonists (SERBAs). Part 4: Functionalization of the benzopyran A-ring

Norman, Bryan H.,Richardson, Timothy I.,Dodge, Jeffrey A.,Pfeifer, Lance A.,Durst, Gregory L.,Wang, Yong,Durbin, Jim D.,Krishnan, Venkatesh,Dinn, Sean R.,Liu, Shengquan,Reilly, John E.,Ryter, Kendal T.

, p. 5082 - 5085 (2008/03/14)

Benzopyrans are selective estrogen recep...

3333-25-3 Process route

1-acetoxy-2,6-dibromo-4-methoxyphenol
2423-74-7

1-acetoxy-2,6-dibromo-4-methoxyphenol

2,6-dibromohydroquinone
3333-25-3

2,6-dibromohydroquinone

Conditions
Conditions Yield
1-acetoxy-2,6-dibromo-4-methoxyphenol; With trimethylsilyl iodide; In acetonitrile; Heating / reflux;
With water; In acetonitrile; at 0 ℃;
98%
With dichloromethane; boron tribromide; at 20 ℃; for 17h; regioselective reaction;
55%
With trimethylsilyl iodide; In acetonitrile;
2,6-dibromo-1,4-benzoquinone
19643-45-9

2,6-dibromo-1,4-benzoquinone

2,6-dibromohydroquinone
3333-25-3

2,6-dibromohydroquinone

Conditions
Conditions Yield
With sulfur dioxide;
With tin(ll) chloride;
With sodium tetrahydroborate;
With methanol; sodium tetrahydroborate; In chloroform; for 0.166667h;
16.1 g

3333-25-3 Upstream products

  • 3958-82-5
    3958-82-5

    2-bromo-1,4-benzoquinone

  • 608-33-3
    608-33-3

    2,6-dibromophenol

  • 19643-45-9
    19643-45-9

    2,6-dibromo-1,4-benzoquinone

  • 123-31-9
    123-31-9

    hydroquinone

3333-25-3 Downstream products

  • 19643-45-9
    19643-45-9

    2,6-dibromo-1,4-benzoquinone

  • 13670-73-0
    13670-73-0

    3,5-dibromo-4-methoxyphenol

  • 74076-59-8
    74076-59-8

    2,6-dibromo-1,4-dimethoxybenzene

  • 13670-72-9
    13670-72-9

    3,5-Dibrom-4-benzyloxy-phenol

Related Products