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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)-

Benzenemethanamine, N-hydroxy-N-(phenylmethyl)-

ON(Cc1ccccc1)Cc1ccccc1 Request for Quotation
Chemical Name: Benzenemethanamine, N-hydroxy-N-(phenylmethyl)-
CAS Number: 621-07-8
Product Number: AG003SIL(AGN-PC-0JL8XP)
Synonyms:
MDL No:
Molecular Formula: C14H15NO
Molecular Weight: 213.2750

Identification/Properties

Properties
MP:
125-128 °C(lit.);
BP:
379.7°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Refractive Index:
1.5300 (estimate)
Computed Properties
Molecular Weight:
213.28g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
213.115g/mol
Monoisotopic Mass:
213.115g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
163
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzenemethanamine, N-hydroxy-N-(phenylmethyl)-, also known as N-hydroxybenzylamine, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the synthesis of various organic molecules due to its unique reactivity and functional groups.In chemical synthesis, Benzenemethanamine, N-hydroxy-N-(phenylmethyl)- can act as a precursor for the introduction of the hydroxylamine moiety into target molecules. This hydroxylamine functional group can participate in a variety of reactions, including nucleophilic substitution, oximation, and rearrangement reactions. Additionally, the phenylmethyl group attached to the hydroxylamine enhances the compound's stability and allows for further functionalization.This compound finds applications in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its ability to introduce the hydroxylamine group selectively and efficiently makes it a valuable reagent in organic synthesis. Researchers and chemists use Benzenemethanamine, N-hydroxy-N-(phenylmethyl)- as a key intermediate in the preparation of complex molecules with specific functionalities, making it an indispensable tool in modern chemical synthesis strategies.