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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-nitrophenyl)methyl]-, monohydrochloride

NOCc1ccc(cc1)[N+](=O)[O-].Cl Request for Quotation
Chemical Name: Hydroxylamine, O-[(4-nitrophenyl)methyl]-, monohydrochloride
CAS Number: 2086-26-2
Product Number: AG002JSU(AGN-PC-0QWOWL)
Synonyms:
MDL No:
Molecular Formula: C7H9ClN2O3
Molecular Weight: 204.6110

Identification/Properties

Properties
MP:
215 °C (dec.)(lit.)
BP:
226°C
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Stability:
Moisture & Light Sensitive
Computed Properties
Molecular Weight:
204.61g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
204.03g/mol
Monoisotopic Mass:
204.03g/mol
Topological Polar Surface Area:
81.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
149
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:
2
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-Nitrobenzyl)hydroxylamine hydrochloride is widely utilized in chemical synthesis as a versatile reagent with multiple applications. This compound is commonly employed as a valuable building block in organic synthesis due to its ability to undergo various chemical reactions and form new chemical entities. Its primary function lies in its role as a key intermediate in the preparation of diverse compounds in the pharmaceutical and agrochemical industries.One of the key applications of O-(4-Nitrobenzyl)hydroxylamine hydrochloride is in the synthesis of various heterocyclic compounds, which are essential structural motifs found in many biologically active molecules. By using this compound as a starting material, chemists can efficiently access a wide range of heterocycles, which are crucial for drug development and molecular research.Furthermore, O-(4-Nitrobenzyl)hydroxylamine hydrochloride serves as a key reagent in the synthesis of nitrones, which are valuable intermediates in organic chemistry. Nitrones can participate in a variety of reactions, such as 1,3-dipolar cycloadditions, providing access to diverse chemical structures with high stereocontrol.Overall, O-(4-Nitrobenzyl)hydroxylamine hydrochloride plays a pivotal role in chemical synthesis, enabling the construction of complex molecules and facilitating the development of innovative compounds with potential applications in various industries.