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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)-

Acetic acid, dibromochloro-

OC(=O)C(Br)(Br)Cl Request for Quotation
Chemical Name: Acetic acid, dibromochloro-
CAS Number: 5278-95-5
Product Number: AG00DESP(AGN-PC-0JLJY0)
Synonyms:
MDL No:
Molecular Formula: C2HBr2ClO2
Molecular Weight: 252.28914

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Chemical Structure


Dibromochloroacetic acid is a valuable compound widely used in chemical synthesis for its unique properties and versatile applications. This acid is commonly employed as a reagent in organic chemistry reactions due to its ability to act as both a halogenating and carboxylating agent. In particular, dibromochloroacetic acid is utilized in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its selective halogenation capabilities make it a key component in the preparation of complex organic molecules with specific functional groups. Furthermore, this compound is prized for its role in the modification of biomolecules and the development of novel materials. Overall, dibromochloroacetic acid plays a crucial role in advancing chemical synthesis by enabling the creation of diverse and tailored chemical structures for a wide range of applications.