1. Home
  2. 3-oxo-4H-1,4-benzoxazine-8-carbaldehyde

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

3-oxo-4H-1,4-benzoxazine-8-carbaldehyde

O=Cc1cccc2c1OCC(=O)N2 Request for Quotation
Chemical Name: 3-oxo-4H-1,4-benzoxazine-8-carbaldehyde
CAS Number: 935758-15-9
Product Number: AG00IHOD(AGN-PC-0CMLDR)
Synonyms:
MDL No:
Molecular Formula: C9H7NO3
Molecular Weight: 177.15678

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-Oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-8-carbaldehyde is a versatile compound widely used in chemical synthesis due to its unique chemical properties. In organic chemistry, this compound serves as a key building block for the synthesis of various heterocyclic compounds. Its α,β-unsaturated structure makes it a valuable intermediate in the formation of complex molecules, allowing for the introduction of functional groups and stereochemical control. Furthermore, the aldehyde group in this compound can participate in various reactions such as condensation, reduction, and nucleophilic addition, expanding its utility in a range of synthetic transformations. Overall, 3-Oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-8-carbaldehyde plays a crucial role in enabling the efficient and precise construction of diverse chemical structures in organic synthesis.