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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, 5-bromo-2,4-dimethoxy-

COc1cc(OC)c(cc1C=O)Br Request for Quotation
Chemical Name: Benzaldehyde, 5-bromo-2,4-dimethoxy-
CAS Number: 130333-46-9
Product Number: AG003MGK(AGN-PC-0JUO86)
Synonyms:
MDL No:
Molecular Formula: C9H9BrO3
Molecular Weight: 245.0700

Identification/Properties

Properties
MP:
140-141 °C(lit.)
BP:
344.3±37.0 °C(Predicted)
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
245.072g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
243.974g/mol
Monoisotopic Mass:
243.974g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
174
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


5-Bromo-2,4-dimethoxybenzaldehyde is a versatile chemical compound commonly utilized in chemical synthesis processes. This compound serves as a key building block in the creation of various organic compounds, thanks to its unique structure and reactivity. Its application in chemical synthesis spans across multiple industries, including pharmaceuticals, agrochemicals, and materials science.In organic synthesis, 5-Bromo-2,4-dimethoxybenzaldehyde can act as a valuable intermediate in the preparation of diverse heterocyclic compounds and complex organic molecules. Its aldehyde functional group allows for further derivatization through various chemical reactions, such as Grignard reactions, Wittig reactions, and Suzuki couplings. The presence of both bromine and methoxy groups enhances the compound's compatibility with a wide range of organic reactions, providing synthetic chemists with ample opportunities to tailor structures for specific applications.Moreover, the unique properties of 5-Bromo-2,4-dimethoxybenzaldehyde make it an essential component in the design and synthesis of bioactive compounds, including pharmaceutical drugs and pesticides. Its structural features contribute to the biological activity and target specificity of these synthesized compounds, making it a valuable tool in drug discovery and development programs.Overall, the versatile nature of 5-Bromo-2,4-dimethoxybenzaldehyde in chemical synthesis enables its widespread use as a critical reagent for the construction of diverse organic molecules with tailored properties and functionalities. Its applications in the synthesis of pharmaceuticals, agrochemicals, and materials highlight its significance in advancing scientific research and industrial processes.