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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)-

Propane, 1,2-dibromo-3-chloro-

ClCC(CBr)Br Request for Quotation
Chemical Name: Propane, 1,2-dibromo-3-chloro-
CAS Number: 96-12-8
Product Number: AG003DDM(AGN-PC-00JTGS)
Synonyms:
MDL No:
Molecular Formula: C3H5Br2Cl
Molecular Weight: 236.3328

Identification/Properties

Properties
BP:
198.6°C at 760 mmHg
Storage:
2-8℃;Inert atmosphere;
Computed Properties
Molecular Weight:
236.331g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
235.843g/mol
Monoisotopic Mass:
233.845g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
32
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


1,2-Dibromo-3-chloropropane, commonly known as DBCP, is a versatile chemical compound with notable applications in chemical synthesis. In organic chemistry, DBCP is frequently utilized as a reagent for halogenation reactions due to its unique properties. This compound serves as an excellent source of both bromine and chlorine atoms, enabling the selective functionalization of organic molecules. Through controlled reactions, DBCP can be introduced into various substrates to create complex structures with specific chemical properties. Its ability to selectively introduce halogens makes it a valuable tool for synthesizing a wide range of organic compounds, including pharmaceutical intermediates, agrochemicals, and materials for industrial applications. The precise reactivity of DBCP in chemical synthesis allows for tailored modifications of organic molecules, offering researchers and chemists a powerful tool for designing and creating new materials with desired properties.