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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)-

1-chloro-3-iodo-2-nitrobenzene

[O-][N+](=O)c1c(Cl)cccc1I Request for Quotation
Chemical Name: 1-chloro-3-iodo-2-nitrobenzene
CAS Number: 937601-42-8
Product Number: AG00H1ZE(AGN-PC-01XFZM)
Synonyms:
MDL No:
Molecular Formula: C6H3ClINO2
Molecular Weight: 283.4510

Identification/Properties

Computed Properties
Molecular Weight:
283.449g/mol
XLogP3:
3
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Chloro-3-iodo-2-nitrobenzene is a versatile compound commonly used in chemical synthesis. It serves as a valuable building block in the creation of a variety of organic compounds due to its unique chemical properties. Specifically, this compound is often employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. In addition, 1-Chloro-3-iodo-2-nitrobenzene has found application in the preparation of complex molecules for research purposes, making it a crucial tool in the field of organic chemistry. Its ability to undergo various transformations and reactions makes it an essential reagent in the development of new compounds with desired properties.