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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)-

1-Anthracenamine,N-phenyl-

c1ccc(cc1)Nc1cccc2c1cc1ccccc1c2 Request for Quotation
Chemical Name: 1-Anthracenamine,N-phenyl-
CAS Number: 98683-00-2
Product Number: AG003TAZ(AGN-PC-0W8HDP)
Synonyms:
MDL No:
Molecular Formula: C20H15N
Molecular Weight: 269.3398

Identification/Properties

Computed Properties
Molecular Weight:
269.347g/mol
XLogP3:
6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
269.12g/mol
Monoisotopic Mass:
269.12g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
333
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Phenyl-1-anthramine is a key compound widely utilized in chemical synthesis, particularly in the field of organic chemistry. Its versatile properties make it a valuable building block in the creation of various advanced materials and pharmaceutical compounds.In chemical synthesis, N-Phenyl-1-anthramine serves as a crucial intermediate in the production of dyes, pigments, and organic molecules. Its unique structure and reactivity enable chemists to incorporate it into complex molecular frameworks, allowing for the development of novel materials with tailored properties. Additionally, N-Phenyl-1-anthramine can participate in a range of chemical reactions, such as coupling reactions and catalytic processes, further expanding its utility in the synthesis of diverse compounds.Overall, the application of N-Phenyl-1-anthramine in chemical synthesis underscores its significance as a versatile and indispensable ingredient for researchers and chemists seeking to design and fabricate advanced materials and pharmaceuticals.