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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)-

3,4-DIBROMOBENZOIC ACID ETHYL ESTER

CCOC(=O)c1ccc(c(c1)Br)Br Request for Quotation
Chemical Name: 3,4-DIBROMOBENZOIC ACID ETHYL ESTER
CAS Number: 60469-88-7
Product Number: AG00EAB9(AGN-PC-0NIDWZ)
Synonyms:
MDL No:
Molecular Formula: C9H8Br2O2
Molecular Weight: 307.9666

Identification/Properties

Computed Properties
Molecular Weight:
307.969g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
307.887g/mol
Monoisotopic Mass:
305.889g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
185
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 3,4-dibromobenzoate is a valuable compound in chemical synthesis. It serves as a key building block in the production of various organic compounds due to its unique chemical properties and reactivity. When used in chemical reactions, Ethyl 3,4-dibromobenzoate can undergo nucleophilic substitution, esterification, or Suzuki coupling reactions, enabling the synthesis of complex organic molecules. This compound is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and materials science, where precise control over the molecular structure is crucial. Additionally, Ethyl 3,4-dibromobenzoate can be utilized as a starting material for the preparation of advanced materials such as liquid crystals, polymers, and dyes. Its versatile nature and compatibility with various synthetic methodologies make it a valuable tool for chemists and researchers in the field of organic chemistry.