2,3-DIBROMO-4,5-DIHYDROXYBENZYL ALCOHOL

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2,3-DIBROMO-4,5-DIHYDROXYBENZYL ALCOHOL

  • Name 2,3-DIBROMO-4,5-DIHYDROXYBENZYL ALCOHOL
  • CAS 4950-06-5
  • Purity 99%
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Product Details

Quality Factory Sells Top Purity 99% 2,3-DIBROMO-4,5-DIHYDROXYBENZYL ALCOHOL 4950-06-5 with Safe Delivery

  • Molecular Formula: C7H6 Br2 O3
  • Molecular Weight: 297.931
  • Vapor Pressure: 2.05E-07mmHg at 25°C 
  • Boiling Point: 408.8°Cat760mmHg 
  • Flash Point: 201°C 
  • PSA: 60.69000 
  • Density: 2.248g/cm3 
  • LogP: 2.11510 

2,3-DIBROMO-4,5-DIHYDROXYBENZYL ALCOHOL(Cas 4950-06-5) Usage

General Description

2,3-Dibromo-4,5-dihydroxybenzyl alcohol, also known as 2,3-Dibromo-4,5-dihydroxybenzyl alcohol, is a chemical compound that is used primarily as an intermediate in organic synthesis. It is a white to off-white solid that is soluble in water and ethanol, and is known for its antibacterial and antiviral properties. It is commonly used as a reagent in the synthesis of pharmaceuticals and other organic compounds. Additionally, 2,3-Dibromo-4,5-dihydroxybenzyl alcohol is used as an antioxidant and preservative in various products, such as cosmetics, food, and pharmaceuticals, due to its ability to inhibit the growth of microorganisms.

InChI:InChI=1/C7H6Br2O3/c8-5-3(2-10)1-4(11)7(12)6(5)9/h1,10-12H,2H2

4950-06-5 Relevant articles

Total synthesis of the biologically active, naturally occurring 3,4-dibromo-5-[2-bromo-3,4-dihydroxy-6-(methoxymethyl)benzyl]benzene-1,2-diol and regioselective O-demethylation of aryl methyl ethers

Akbaba, Yusuf,Balaydin, Halis Tuerker,Goeksu, Sueleyman,Sahin, Ertan,Menzek, Abdullah

experimental part, p. 1127 - 1135 (2010/08/21)

3,4-Dibromo-5-[2-bromo-3,4-dihydroxy-6-(...

In-vitro cytotoxic activities of the major bromophenols of the red alga Polysiphonia lanosa and some novel synthetic isomers

Shoeib, Nagwa A.,Bibby, Michael C.,Blunden, Gerald,Linley, Peter A.,Swaine, David J.,Wheelhouse, Richard T.,Wright, Colin W.

, p. 1445 - 1449 (2007/10/03)

Bioassay-guided fractionation was applie...

Synthesis of some hydroxymethylbromophenols of marine origin

Sudalai, A.,Rao, G. S. Krishna

, p. 858 - 859 (2007/10/02)

The hydroxymethylbromophenols 5, 7 and 9...

4950-06-5 Process route

2,3-dibromo-4,5-dihydroxybenzylaldehyde
14045-41-1

2,3-dibromo-4,5-dihydroxybenzylaldehyde

lanosol
4950-06-5

lanosol

Conditions
Conditions Yield
With sodium tetrahydroborate; In methanol;
88%
With potassium borohydride;
With potassium borohydride;
2,3-dibromo-4,5-dimethoxy-1-(methoxymethyl)benzene

2,3-dibromo-4,5-dimethoxy-1-(methoxymethyl)benzene

lanosol
4950-06-5

lanosol

Conditions
Conditions Yield
With boron tribromide; In dichloromethane; at 0 - 25 ℃; Inert atmosphere;

4950-06-5 Upstream products

  • 14045-41-1
    14045-41-1

    2,3-dibromo-4,5-dihydroxybenzylaldehyde

  • 40089-29-0
    40089-29-0

    dipotassium 2,3-dibromo-5-hydroxybenzyl-1',4-disulfate

  • 2973-75-3
    2973-75-3

    5,6-dibromo-4-hydroxy-3-methoxybenzaldehyde

  • 2973-76-4
    2973-76-4

    5-bromo-4-hydroxy-3-methoxybenzaldehyde

4950-06-5 Downstream products

  • 100676-08-2
    100676-08-2

    methylrhodomelol

  • 100676-10-6
    100676-10-6

    rhodomelol

  • 54502-93-1
    54502-93-1

    3,4-dibromo-5-(ethoxymethyl)benzene-1,2-diol

  • 70625-32-0
    70625-32-0

    3,4-Dibrom-5,5'-methylendibrenzcatechin

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