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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)-

4-Pyridinamine, 2-chloro-5-fluoro-3-nitro-

[O-][N+](=O)c1c(Cl)ncc(c1N)F Request for Quotation
Chemical Name: 4-Pyridinamine, 2-chloro-5-fluoro-3-nitro-
CAS Number: 405230-90-2
Product Number: AG00C6DV(AGN-PC-03NBVP)
Synonyms:
MDL No:
Molecular Formula: C5H3ClFN3O2
Molecular Weight: 191.5476

Identification/Properties

Computed Properties
Molecular Weight:
191.546g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
190.99g/mol
Monoisotopic Mass:
190.99g/mol
Topological Polar Surface Area:
84.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
188
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-fluoro-3-nitropyridin-4-amine is a versatile compound widely used in chemical synthesis. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Due to its unique structure and reactivity, this compound plays a crucial role in the development of new materials and substances with enhanced properties. It can undergo a wide range of chemical reactions, including substitution, addition, and coupling reactions, making it a valuable intermediate in organic synthesis. Its applications extend to the production of dyes, pigments, and other specialty chemicals, showcasing its importance in the field of chemistry.