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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzaldehyde, 4-bromo-3-hydroxy-

O=Cc1ccc(c(c1)O)Br Request for Quotation
Chemical Name: Benzaldehyde, 4-bromo-3-hydroxy-
CAS Number: 20035-32-9
Product Number: AG002CPG(AGN-PC-002G9J)
Synonyms:
MDL No:
Molecular Formula: C7H5BrO2
Molecular Weight: 201.0174

Identification/Properties

Computed Properties
Molecular Weight:
201.019g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
199.947g/mol
Monoisotopic Mass:
199.947g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
127
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-3-hydroxybenzaldehyde is a versatile compound widely used in chemical synthesis due to its unique properties. This compound plays a crucial role in various reactions and is particularly valued for its reactivity and ability to introduce functional groups into organic molecules. In organic synthesis, 4-Bromo-3-hydroxybenzaldehyde serves as a key building block for the construction of complex organic molecules. Its aldehyde group allows for the formation of new carbon-carbon bonds through various reactions such as nucleophilic addition and condensation reactions. Additionally, the bromine atom present in the compound can further enhance its reactivity by participating in substitution reactions. Overall, the incorporation of 4-Bromo-3-hydroxybenzaldehyde in chemical synthesis enables the creation of diverse compounds with unique structural and chemical properties, making it an essential component in the toolkit of synthetic chemists worldwide.