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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)-

Methane, bromochloronitro-

[O-][N+](=O)C(Br)Cl Request for Quotation
Chemical Name: Methane, bromochloronitro-
CAS Number: 135531-25-8
Product Number: AG007ZIY(AGN-PC-0JT9KC)
Synonyms:
MDL No:
Molecular Formula: CHBrClNO2
Molecular Weight: 174.3811

Identification/Properties

Computed Properties
Molecular Weight:
174.378g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
172.888g/mol
Monoisotopic Mass:
172.888g/mol
Topological Polar Surface Area:
45.8A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
61.1
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


Bromochloronitromethane, also known as N-Bromoacetamide, is a versatile reagent widely used in chemical synthesis for various purposes. One of its key applications is in organic transformations, where it acts as a selective halogenating agent. Due to its unique reactivity, Bromochloronitromethane is particularly effective in introducing halogen groups, such as bromine and chlorine, into organic molecules. This selective halogenation plays a crucial role in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals, allowing chemists to easily modify and functionalize organic compounds with precision. Additionally, Bromochloronitromethane can also be utilized in the preparation of heterocyclic compounds and as a valuable building block in organic synthesis strategies. Its ability to facilitate controlled halogenation reactions makes it a valuable tool for chemists seeking to design and create complex organic molecules for various applications.