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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-(2-chloro-5-nitrophenyl)-

CC(=O)c1cc(ccc1Cl)N(=O)=O Request for Quotation
Chemical Name: Ethanone, 1-(2-chloro-5-nitrophenyl)-
CAS Number: 23082-50-0
Product Number: AG003GZD(AGN-PC-0JLYD5)
Synonyms:
MDL No:
Molecular Formula: C8H6ClNO3
Molecular Weight: 199.5911

Identification/Properties

Properties
BP:
244.8°C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
199.59g/mol
XLogP3:
2.2
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2′-Chloro-5′-nitroacetophenone is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and functional materials. One key application of 2′-Chloro-5′-nitroacetophenone is as a precursor in the production of nitro-substituted aromatic compounds. Its nitro group can undergo a range of chemical transformations, such as reduction, oxidation, and substitution reactions, enabling the synthesis of diverse organic molecules with tailored functionalities. Furthermore, the chloro group in 2′-Chloro-5′-nitroacetophenone can participate in cross-coupling reactions, facilitating the formation of carbon-carbon or carbon-heteroatom bonds. Overall, the strategic incorporation of 2′-Chloro-5′-nitroacetophenone in chemical synthesis offers synthetic chemists a powerful tool to access structurally complex and biologically relevant compounds of interest.