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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)-

(R)-1-(2-Nitrophenyl)ethanamine hydrochloride

[O-][N+](=O)c1ccccc1[C@H](N)C.Cl Request for Quotation
Chemical Name: (R)-1-(2-Nitrophenyl)ethanamine hydrochloride
CAS Number: 1431699-56-7
Product Number: AG009FW8(AGN-PC-0WAMBH)
Synonyms:
MDL No: MFCD24411694
Molecular Formula: C8H11ClN2O2
Molecular Weight: 202.6381

Identification/Properties

Computed Properties
Molecular Weight:
202.638g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
202.051g/mol
Monoisotopic Mass:
202.051g/mol
Topological Polar Surface Area:
71.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
167
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzenemethanamine, α-methyl-2-nitro-, hydrochloride (1:1), (αR)- is a versatile compound commonly used in chemical synthesis due to its unique properties and reactivity. This compound is particularly valuable in organic chemistry as a key intermediate in the synthesis of various pharmaceuticals and fine chemicals. Its chirality, with the αR configuration, plays a crucial role in controlling the stereochemistry of reactions it is involved in, leading to the formation of specific enantiomers essential in drug design and development. Its nitro group allows for further functionalization through reduction or substitution reactions, expanding its synthetic utility in creating diverse molecular structures. In addition, the presence of the hydrochloride salt facilitates purification processes and enhances solubility in polar solvents, making it easier to handle in laboratory settings. Whether employed as a catalyst, a building block, or a precursor, Benzenemethanamine, α-methyl-2-nitro-, hydrochloride (1:1), (αR)- is a valuable tool for researchers and chemists alike seeking to synthesize complex molecules with precision and efficiency.