4693-01-0

Basic information

• Product Name: 1-methyl-6-nitro-2H-3,1-benzoxazine-2,4(1H)-dione
• Synonyms: 1-methyl-6-nitro-2H-3,1-benzoxazine-2,4(1H)-dione;2H-3,1-Benzoxazine-2,4(1H)-dione, 1-methyl-6-nitro-;5-Nitro-N-methylisatoic anhydride;Einecs 225-150-6
• CAS NO: 4693-01-0
• Molecular Formula: C₉H₆N₂O₅
• Molecular Weight: 222.15434
• EINECS: 225-150-6
• Mol File: 4693-01-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 392.4°Cat760mmHg
• Flash Point: 191.1°C
• Appearance: /
• Density: 1.551g/cm³
• Vapor Pressure: 2.3E-06mmHg at 25°C
• Refractive Index: 1.623
• CAS DataBase Reference: 1-methyl-6-nitro-2H-3,1-benzoxazine-2,4(1H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-6-nitro-2H-3,1-benzoxazine-2,4(1H)-dione(4693-01-0)
• EPA Substance Registry System: 1-methyl-6-nitro-2H-3,1-benzoxazine-2,4(1H)-dione(4693-01-0)

Safety Data

• Hazardous Substances Data: 4693-01-0(Hazardous Substances Data)

Usage

General Description

1-methyl-6-nitro-2H-3,1-benzoxazine-2,4(1H)-dione is a chemical compound with the molecular formula C9H6N2O5. It is a nitro-substituted benzoxazine derivative with a cyclic structure. 1-methyl-6-nitro-2H-3,1-benzoxazine-2,4(1H)-dione is a yellow solid at room temperature and is commonly used in the synthesis of various organic compounds. It is also known for its potential pharmaceutical applications, including as a building block for drug development. However, due to its nitro group, it is important to handle this compound with caution as nitro compounds can be potentially explosive and reactive.

InChI:InChI=1/C9H6N2O5/c1-10-7-3-2-5(11(14)15)4-6(7)8(12)16-9(10)13/h2-4H,1H3

Upstream product

• 541-41-3 chloroformic acid ethyl ester 
• 77-78-1 dimethyl sulfate 
• 616-79-5 2-amino-5-nitro-benzoic acid 
• 4693-02-1 6-nitroisatoic anhydride 
• 74-88-4 methyl iodide 

Downstream Products

• 77423-11-1 2-Methylamino-5-nitro-benzoic acid hydrazide 
• 77423-09-7 5-amino-2-methylaminobenzoic acid hydrazide 
• 77422-98-1 7-(acetylamino)-4,9-dihydro-4-methyl-9-oxopyrazolo<5,1-b>quinazoline-2-carboxylic acid 
• 77422-99-2 PD 90780 
• 1032571-34-8 spiro{(1',4'-anhydro-2',3',5'-tri-O-benzyl-D-arabinitol)-1',2-[(11aR)-7-nitro-10-methylpyrrolo[2,1-c][1,4]benzodiazepine-5,11-dione]} 
• 1268263-73-5 spiro{(1',4'-anhydro-2',3',5'-tri-O-benzyl-L-arabinitol)-1',2-[(11aS)-7-nitro-10-methylpyrrolo[2,1-c][1,4]benzodiazepine-5,11-dione]} 
• 1356111-73-3 tert-butyl 5-amino-2-(methylamino)benzoate 
• 1609243-43-7 tert-butyl 5-(3-{[2-(1-{5-[(3aS,4S,6aR)-2-oxo-hexahydro-1H-thieno[3,4-d]imidazolidin-4-yl]pentanamido}-3,6,9,12-tetraoxapentadecan-15-amido)ethyl]disulfanyl}propanamido)-2-(methylamino)benzoate 
• 1609243-42-6 tert-butyl 2-(methylamino)-5-nitrobenzoate 

Relevant articles and documents

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Into Deep Water: Optimizing BCL6 Inhibitors by Growing into a Solvated Pocket

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Biotin-conjugated N-methylisatoic anhydride: A chemical tool for nucleic acid separation by selective 2′-hydroxyl acylation of RNA

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