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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)-

Ethanone, 1-(5-chloro-2-nitrophenyl)-

Clc1ccc(c(c1)C(=O)C)[N+](=O)[O-] Request for Quotation
Chemical Name: Ethanone, 1-(5-chloro-2-nitrophenyl)-
CAS Number: 18640-60-3
Product Number: AG00ACYM(AGN-PC-0JNSWO)
Synonyms:
MDL No:
Molecular Formula: C8H6ClNO3
Molecular Weight: 199.5911

Identification/Properties

Computed Properties
Molecular Weight:
199.59g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
199.004g/mol
Monoisotopic Mass:
199.004g/mol
Topological Polar Surface Area:
62.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
226
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(5-Chloro-2-nitrophenyl)ethanone is a versatile compound used in chemical synthesis for its unique properties and reactivity. With its distinctive chlorine and nitro groups, this compound serves as a valuable building block in the creation of various organic molecules.One of the key applications of 1-(5-Chloro-2-nitrophenyl)ethanone is in the synthesis of pharmaceutical intermediates. By utilizing the reactive functional groups present in this compound, chemists can introduce specific structural motifs necessary for the development of new drugs. This compound can be instrumental in the production of bioactive compounds with potential therapeutic applications.Furthermore, 1-(5-Chloro-2-nitrophenyl)ethanone can also be employed in the preparation of agrochemicals. By incorporating this compound into the molecular structure of pesticides or herbicides, researchers can enhance the effectiveness and selectivity of these crop protection products. The presence of the chloro and nitro substituents can confer desired properties such as improved solubility or enhanced biological activity.In addition, this compound plays a crucial role in material science and polymer chemistry. By utilizing 1-(5-Chloro-2-nitrophenyl)ethanone as a precursor, chemists can create functionalized polymers with tailored properties. These polymers may exhibit specific characteristics such as conductivity, optical activity, or mechanical strength, making them suitable for a wide range of industrial applications.Overall, the application of 1-(5-Chloro-2-nitrophenyl)ethanone in chemical synthesis spans across various fields, including pharmaceuticals, agrochemicals, and materials science. Its versatility and reactivity make it a valuable tool for the design and development of novel compounds with diverse functionalities and applications.