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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)-

1,4-Benzenedicarboxylic acid, 2,5-dibromo-, dimethyl ester

COC(=O)c1cc(Br)c(cc1Br)C(=O)OC Request for Quotation
Chemical Name: 1,4-Benzenedicarboxylic acid, 2,5-dibromo-, dimethyl ester
CAS Number: 18014-00-1
Product Number: AG0021Q6(AGN-PC-0JLWRO)
Synonyms:
MDL No:
Molecular Formula: C10H8Br2O4
Molecular Weight: 351.9761

Identification/Properties

Computed Properties
Molecular Weight:
351.978g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
351.877g/mol
Monoisotopic Mass:
349.879g/mol
Topological Polar Surface Area:
52.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
254
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-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


The chemical compound 1,4-Benzenedicarboxylic acid, 2,5-dibromo-, 1,4-dimethyl ester plays a crucial role in various chemical synthesis processes. It is commonly employed as a building block in the production of polymers, particularly in the manufacture of high-performance engineering plastics. This compound serves as a key intermediate in the synthesis of polyesters and polyamides, imparting desirable properties such as high thermal stability and chemical resistance to the final polymer products. Additionally, its chemical structure allows for facile manipulation and functionalization, enabling tailored modifications to suit specific application requirements in industries such as automotive, aerospace, and electronics. Its versatile nature and compatibility with other monomers make it a valuable asset in the arsenal of synthetic chemists seeking to create novel materials with tailored properties and performance characteristics.