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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, 1-chloro-2-iodo-3-nitro-

[O-][N+](=O)c1cccc(c1I)Cl Request for Quotation
Chemical Name: Benzene, 1-chloro-2-iodo-3-nitro-
CAS Number: 32337-97-6
Product Number: AG0032QM(AGN-PC-03URBP)
Synonyms:
MDL No:
Molecular Formula: C6H3ClINO2
Molecular Weight: 283.4510

Identification/Properties

Properties
MP:
100-101°C
BP:
305.0±27.0°C at 760 mmHg
Storage:
Light sensitive;Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
283.449g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
282.89g/mol
Monoisotopic Mass:
282.89g/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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Chloro-2-iodo-3-nitrobenzene is commonly utilized in chemical synthesis as a versatile building block due to its unique chemical properties. This compound serves as a valuable starting material for the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and fine chemicals. Its strategic placement of different functional groups allows for efficient manipulation and introduction of additional substituents through various chemical reactions. Specifically, 1-Chloro-2-iodo-3-nitrobenzene is frequently employed in the synthesis of complex heterocyclic compounds, biologically active molecules, and dyes. Its ability to undergo diverse chemical transformations makes it a crucial intermediate in the development of novel organic compounds with desired properties.