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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)-

2(1H)-Pyridinone, 3-amino-5-chloro-

Nc1cc(Cl)c[nH]c1=O Request for Quotation
Chemical Name: 2(1H)-Pyridinone, 3-amino-5-chloro-
CAS Number: 98027-36-2
Product Number: AG003IWB(AGN-PC-03CU7P)
Synonyms:
MDL No: MFCD07375031
Molecular Formula: C5H5ClN2O
Molecular Weight: 144.5590

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
144.558g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
144.009g/mol
Monoisotopic Mass:
144.009g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
207
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


3-Amino-5-chloropyridin-2(1H)-one, also known as $name$, serves a crucial role in chemical synthesis as a versatile building block for the development of various organic compounds. Its unique structure and reactivity make it a valuable tool for the creation of complex molecules in the field of medicinal chemistry, agrochemicals, and materials science.One significant application of 3-Amino-5-chloropyridin-2(1H)-one is its use as a key intermediate in the synthesis of pharmaceutical compounds. By incorporating this compound into the molecular structure of drug candidates, chemists can modify their pharmacological properties, such as enhancing bioavailability or targeting specific biological pathways. This process allows for the tailored design of drugs with improved efficacy and reduced side effects.Furthermore, 3-Amino-5-chloropyridin-2(1H)-one can be utilized in the preparation of agrochemicals by enabling the synthesis of active ingredients for crop protection products. The compound's functional groups and reactivity enable the introduction of desired features, such as pesticidal or herbicidal properties, into the final agricultural formulations. This application underscores the importance of 3-Amino-5-chloropyridin-2(1H)-one in the development of sustainable agricultural solutions.In the realm of materials science, 3-Amino-5-chloropyridin-2(1H)-one can be employed to construct advanced polymers, dyes, and functional materials with tailored properties. Through controlled chemical reactions, scientists can incorporate this compound into the backbone of polymeric structures or as a functional group for specific applications, such as sensors or electronic devices. This versatility highlights the potential of 3-Amino-5-chloropyridin-2(1H)-one as a valuable building block for creating novel materials with diverse functionalities.