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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)-

Benzene, 2-bromo-1-chloro-3-nitro-

[O-][N+](=O)c1cccc(c1Br)Cl Request for Quotation
Chemical Name: Benzene, 2-bromo-1-chloro-3-nitro-
CAS Number: 19128-48-4
Product Number: AG002F5N(AGN-PC-03MUV5)
Synonyms:
MDL No:
Molecular Formula: C6H3BrClNO2
Molecular Weight: 236.4505

Identification/Properties

Properties
MP:
83-85℃
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
236.449g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
234.904g/mol
Monoisotopic Mass:
234.904g/mol
Topological Polar Surface Area:
45.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
161
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-1-chloro-3-nitrobenzene is a valuable compound widely utilized in chemical synthesis for various applications. As a versatile building block in organic chemistry, it serves as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical structure enables it to participate in diverse chemical reactions, such as nucleophilic substitution, Suzuki coupling, and Heck reactions, facilitating the synthesis of complex molecules with precision and efficiency. With its selective reactivity towards different functional groups, 2-Bromo-1-chloro-3-nitrobenzene plays a crucial role in the design and synthesis of novel compounds with tailored properties and functionalities, making it an indispensable tool for modern organic synthesis strategies.