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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)-

1,3-dihydro-3-benzazepin-2-one

O=C1NC=Cc2c(C1)cccc2 Request for Quotation
Chemical Name: 1,3-dihydro-3-benzazepin-2-one
CAS Number: 19301-09-8
Product Number: AG003EDF(AGN-PC-0L7ELC)
Synonyms:
MDL No: MFCD01101239
Molecular Formula: C10H9NO
Molecular Weight: 159.1846

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
159.188g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
159.068g/mol
Monoisotopic Mass:
159.068g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
210
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
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Benzo[d]azepin-2(3H)-one, also known as dibenzazepinone, is a versatile compound commonly utilized in chemical synthesis for its unique structural features. This heterocyclic molecule contains a benzene ring fused to a seven-membered nitrogen-containing ring, making it a valuable building block in the development of pharmaceuticals, agrochemicals, and advanced materials. In organic synthesis, 1H-Benzo[d]azepin-2(3H)-one can undergo various functionalization reactions to introduce substituents at different positions on the ring system, enabling the creation of diverse derivatives with potential biological activities. This compound serves as a key intermediate in the preparation of biologically active compounds such as antipsychotic agents, antidepressants, and anti-inflammatory drugs. Additionally, its structural flexibility and reactivity make it a valuable tool for exploring new synthetic methodologies and designing novel molecules with targeted properties. As a pivotal component in the synthesis of complex organic molecules, 1H-Benzo[d]azepin-2(3H)-one plays a crucial role in advancing the field of organic chemistry and drug discovery.