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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)-

Hydroxylamine, O-[4-nitro-2-(trifluoromethyl)phenyl]-

NOc1ccc(cc1C(F)(F)F)[N+](=O)[O-] Request for Quotation
Chemical Name: Hydroxylamine, O-[4-nitro-2-(trifluoromethyl)phenyl]-
CAS Number: 94832-15-2
Product Number: AG003TFC(AGN-PC-00FX2O)
Synonyms:
MDL No: MFCD18070977
Molecular Formula: C7H5F3N2O3
Molecular Weight: 222.1214

Identification/Properties

Properties
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
222.123g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
1
Exact Mass:
222.025g/mol
Monoisotopic Mass:
222.025g/mol
Topological Polar Surface Area:
81.1A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
241
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


O-[4-Nitro-2-(trifluoromethyl)phenyl]hydroxylamine is a valuable compound in chemical synthesis due to its unique properties. It serves as an important reagent for the introduction of functional groups in organic molecules. This compound is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its ability to selectively react with specific functional groups makes it a versatile building block in the creation of complex organic compounds. Furthermore, O-[4-Nitro-2-(trifluoromethyl)phenyl]hydroxylamine plays a crucial role in the development of novel chemical entities with enhanced properties for various industrial applications. Its application in chemical synthesis enables the efficient production of diverse molecules with tailored functionalities and improved performance characteristics.