ChemicalBook--->CAS DataBase List--->89976-75-0

89976-75-0

89976-75-0 Structure

89976-75-0 Structure
IdentificationBack Directory
[Name]

6-AMINO-2H-1,4-BENZOXAZIN-3(4H)-ONE
[CAS]

89976-75-0
[Synonyms]

6-amino-4H-1,4-benzoxazin-3-one
6-AMINO-4H-BENZO[1,4]OXAZIN-3-ONE
6-Amino-2H-1,4-benzoxin-3(4H)-one
6-AMINO-2H-1,4-BENZOXAZIN-3(4H)-ONE
2H-1,4-benzoxazin-3(4H)-one, 6-amino-
6-Amino-2H-1,4-benzoxazin-3(4H)-one 97%
6-amino-2,4-dihydro-1,4-benzoxazin-3-one
6-Amino-3-oxo-3,4-dihydrobenzo[1,4]oxazine
6-AMino-3,4-dihydro-2H-1,4-benzoxazin-3-one
6-Amino-3,4-dihydro-3-oxo-2H-1,4-benzoxazine
6-amino-2H-1,4-benzoxazin-3(4H)-one(SALTDATA: FREE)
[Molecular Formula]

C8H8N2O2
[MDL Number]

MFCD03425742
[MOL File]

89976-75-0.mol
[Molecular Weight]

164.16
Chemical PropertiesBack Directory
[Melting point ]

266-268°C
[density ]

1.344
[storage temp. ]

2-8°C
[form ]

solid
[color ]

Pale brown
[InChI]

1S/C8H8N2O2/c9-5-1-2-7-6(3-5)10-8(11)4-12-7/h1-3H,4,9H2,(H,10,11)
[InChIKey]

GEPGYMHEMLZMBC-UHFFFAOYSA-N
[SMILES]

Nc1ccc2OCC(=O)Nc2c1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P301+P312-P302+P352-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

36/37/38-52-22
[Safety Statements ]

26-36/37/39-24/25
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

29349990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Spectrum DetailBack Directory
[Spectrum Detail]

6-AMINO-2H-1,4-BENZOXAZIN-3(4H)-ONE(89976-75-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-NITRO-2H-1,4-BENZOXAZIN-3(4H)-ONE

81721-87-1

6-AMINO-2H-1,4-BENZOXAZIN-3(4H)-ONE

89976-75-0

General procedure for the synthesis of 6-amino-2H-1,4-benzomorpholin-3(4H)-one from 6-nitro-2H-1,4-benzoxazin-3(4H)-one: to a solution of 6-nitro-2H-1,4-benzoxazin-3(4H)-one (2.97 g, 15.00 mmol) in methanol (50 mL) was added 10% palladium/carbon catalyst (0.30 g). The reaction mixture was stirred under hydrogen atmosphere for 16 hours. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated to afford 6-amino-2H-1,4-benzomorpholin-3(4H)-one (2.36 g, 95% yield) as a brown solid. Mass spectrometry (MS) analysis showed a molecular ion peak of 165 (M + H).

[References]

[1] ChemCatChem, 2014, vol. 6, # 11, p. 3153 - 3159
[2] Patent: WO2018/19252, 2018, A1. Location in patent: Page/Page column 37
[3] ChemSusChem, 2017, vol. 10, # 15, p. 3035 - 3039
[4] Journal of Medicinal Chemistry, 2005, vol. 48, # 1, p. 71 - 90
[5] Patent: US2009/298819, 2009, A1. Location in patent: Page/Page column 16; 22
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