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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)-

Methyl2-bromo-4-methoxybenzoate

COc1ccc(c(c1)Br)C(=O)OC Request for Quotation
Chemical Name: Methyl2-bromo-4-methoxybenzoate
CAS Number: 17100-65-1
Product Number: AG00784Y(AGN-PC-0WAE55)
Synonyms:
MDL No:
Molecular Formula: C9H9BrO3
Molecular Weight: 245.0700

Identification/Properties

Computed Properties
Molecular Weight:
245.072g/mol
XLogP3:
2.4
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:
184
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-bromo-4-methoxybenzoate is a versatile compound widely utilized in chemical synthesis as a key building block in organic chemistry reactions. This compound serves as an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique chemical structure enables it to participate in diverse transformations, including esterification, nucleophilic substitution, and Suzuki coupling reactions. Methyl 2-bromo-4-methoxybenzoate plays a crucial role in the creation of complex molecules with specific biological or chemical properties, making it a valuable tool for researchers and chemists in the pursuit of new materials and compounds.