CAS 1761-61-1
:5-Bromosalicylaldehyde
Description:
5-Bromosalicylaldehyde is an organic compound characterized by the presence of both a bromine atom and an aldehyde functional group attached to a salicylic acid derivative. Its molecular structure features a bromine substituent at the 5-position of the aromatic ring, along with a formyl group (-CHO) at the 1-position, which contributes to its reactivity and potential applications in organic synthesis. This compound typically appears as a pale yellow to light brown solid and is soluble in organic solvents such as ethanol and ether, but less so in water due to its hydrophobic aromatic nature. 5-Bromosalicylaldehyde is known for its role in various chemical reactions, including nucleophilic substitutions and condensation reactions, making it valuable in the synthesis of pharmaceuticals and agrochemicals. Additionally, it exhibits properties that may be utilized in the development of dyes and other functional materials. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled.
Formula:C7H5BrO2
InChI:InChI=1S/C7H5BrO2/c8-6-1-2-7(10)5(3-6)4-9/h1-4,10H
InChI key:InChIKey=MKKSTJKBKNCMRV-UHFFFAOYSA-N
SMILES:C(=O)C1=C(O)C=CC(Br)=C1
Synonyms:- 2-Hydroxy-5-Bromobenzaldehyde
- 3-Bromo-6-hydroxybenzaldehyde
- 4-Bromo-2-formylphenol
- 5-Br-SALICYLAL
- 5-Br-salycylal
- 5-Bromo-2-hydroxybenzaldehyde
- 5-Bromosalicilaldehido
- 5-Bromsalicylaldehyd
- Akos Bbs-00003168
- Benzaldehyde, 5-bromo-2-hydroxy-
- Nsc 7310
- Nsc 9258
- Otava-Bb Bb7018801955
- Salicylaldehyde, 5-bromo-
- See more synonyms
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Found 9 products.
5-Bromosalicylaldehyde
CAS:Formula:C7H5BrO2Purity:>98.0%(GC)(T)Color and Shape:White to Almost white powder to crystalMolecular weight:201.025-Bromosalicylaldehyde, 98%
CAS:<p>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</p>Formula:C7H5BrO2Purity:98%Color and Shape:Crystals or powder or crystalline powder or lumps, White to cream to brown or pale purpleMolecular weight:201.02Benzaldehyde, 5-bromo-2-hydroxy-
CAS:Formula:C7H5BrO2Purity:98%Color and Shape:SolidMolecular weight:201.01745-Bromo-2-hydroxybenzaldehyde, min. 98%
CAS:Formula:C7H5BrO2Purity:min. 98%Color and Shape:Off white solidMolecular weight:201.025-Bromo-2-hydroxybenzaldehyde
CAS:5-Bromo-2-hydroxybenzaldehydeFormula:C7H5BrO2Purity:98%Color and Shape: faint beige/ brown solidMolecular weight:201.0174g/mol5-Bromosalicylaldehyde
CAS:Formula:C7H5BrO2Purity:98%Color and Shape:Solid, Crystalline Powder or LumpsMolecular weight:201.0195-Bromosalicylaldehyde
CAS:Controlled Product<p>Applications 5-Bromosalicylaldehyde (cas# 1761-61-1) is a compound useful in organic synthesis.<br></p>Formula:C7H5BrO2Color and Shape:NeatMolecular weight:201.025-Bromo-2-hydroxybenzaldehyde
CAS:<p>5-Bromo-2-hydroxybenzaldehyde (5BHB) is an organic compound that has been shown to have a coordination geometry of group p2. This compound binds to DNA and RNA, inhibiting the transcription process. 5BHB also has the ability to form a copper complex with malonic acid. This redox potential is reduced by one electron when copper is added in order to form the copper complex, which allows for the reactivity of 5BHB to be increased. 5BHB binds to nucleic acids through hydrogen bonding interactions with nitrogen atoms and lone pairs on oxygen atoms. The reaction mechanism for 5BHB involves intramolecular hydrogen transfer from one molecule of 5BHB to another, forming an intermediate that then reacts with nucleic acid.</p>Formula:C7H5BrO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:201.02 g/mol5-Bromo-2-hydroxybenzaldehyde
CAS:Formula:C7H5BrO2Purity:98.0 min. %Color and Shape:Off white solidMolecular weight:201.02








