CAS 2973-77-5
:3,5-Dibromo-4-idrossibenzaldeide
- 4-Hydroxy-3,5-dibromobenzaldehyde
- NSC 72944
- Benzaldehyde, 3,5-dibromo-4-hydroxy-
- 3,5-Dibromo-4-hydroxybenzaldehyde
3,5-Dibromo-4-hydroxybenzaldehyde
CAS:Formula:C7H4Br2O2Purezza:>98.0%(GC)(T)Colore e forma:White to Orange to Green powder to crystalPeso molecolare:279.923,5-Dibromo-4-hydroxybenzaldehyde, 97%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formula:C7H4Br2O2Purezza:97%Colore e forma:Crystalline powder or powder or crystals or needles, White to cream to pinkPeso molecolare:279.92Benzaldehyde, 3,5-dibromo-4-hydroxy-
CAS:Formula:C7H4Br2O2Purezza:95%Colore e forma:SolidPeso molecolare:279.91353,5-dibromo-4-hydroxybenzaldehyde
CAS:3,5-dibromo-4-hydroxybenzaldehydeFormula:C7H4Br2O2Purezza:98%Colore e forma: brown solidPeso molecolare:279.91g/mol3,5-Dibromo-4-hydroxybenzaldehyde
CAS:3,5-Dibromo-4-hydroxybenzaldehyde is an aldehyde that is used as a precursor to other organic compounds. It can be produced using the efficient method of reacting 3,5-dibromo-4-hydroxybenzoic acid with sodium borohydride in methanol. The molecule has three hydroxymethyl groups and two functional groups. 3,5-Dibromo-4-hydroxybenzaldehyde is soluble in water and organic solvents such as ethanol and acetone. This compound has shown antibacterial activity against some strains of bacteria, including group P2 bacteria. The reaction yield for the synthesis of this compound is approximately 93%. The inhibitory activities of 3,5-dibromo-4-hydroxybenzaldehyde have been demonstrated against both Gram positive and Gram negative bacteria.
Formula:C7H4Br2O2Purezza:Min. 95%Colore e forma:PowderPeso molecolare:279.91 g/mol3,5-Dibromo-4-hydroxybenzaldehyde
CAS:Formula:C7H4Br2O2Purezza:95%Colore e forma:SolidPeso molecolare:279.915





