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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)-

1H-1,4-Benzodiazepine-2,5-dione, 3,4-dihydro-1-methyl-

O=C1CNC(=O)c2c(N1C)cccc2 Request for Quotation
Chemical Name: 1H-1,4-Benzodiazepine-2,5-dione, 3,4-dihydro-1-methyl-
CAS Number: 1133-42-2
Product Number: AG0081YN(AGN-PC-0KWIHH)
Synonyms:
MDL No:
Molecular Formula: C10H10N2O2
Molecular Weight: 190.1986

Identification/Properties

Computed Properties
Molecular Weight:
190.202g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
190.074g/mol
Monoisotopic Mass:
190.074g/mol
Topological Polar Surface Area:
49.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
265
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


1-Methyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in organic chemistry due to its unique structure and reactivity. $name$ is commonly employed in the synthesis of heterocyclic compounds, pharmaceutical ingredients, and advanced materials. Its utility extends to the development of novel drug molecules, agrochemicals, and functional materials. In chemical synthesis, $name$ acts as a key intermediate, facilitating the creation of diverse molecular structures with desirable properties and functionalities. Its strategic incorporation enables the efficient construction of complex organic frameworks, making it an indispensable tool for synthetic chemists seeking to access a broad range of molecular architectures.