Home Other Building Blocks 1-Methyl-1H-benzo[d][1,3]oxazine-2,4-dione

1-Methyl-1H-benzo[d][1,3]oxazine-2,4-dione

CAS No.:
10328-92-4
Catalog Number:
AG003EH2
Molecular Formula:
C9H7NO3
Molecular Weight:
177.1568
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%(GC)
In Stock USA
United States
$98
- +
25g
98%(GC)
In Stock USA
United States
$254
- +
100g
98%(GC)
In Stock USA
United States
$601
- +
Product Description
Catalog Number:
AG003EH2
Chemical Name:
1-Methyl-1H-benzo[d][1,3]oxazine-2,4-dione
CAS Number:
10328-92-4
Molecular Formula:
C9H7NO3
Molecular Weight:
177.1568
MDL Number:
MFCD00006815
IUPAC Name:
1-methyl-3,1-benzoxazine-2,4-dione
InChI:
InChI=1S/C9H7NO3/c1-10-7-5-3-2-4-6(7)8(11)13-9(10)12/h2-5H,1H3
InChI Key:
KJMRWDHBVCNLTQ-UHFFFAOYSA-N
SMILES:
O=c1oc(=O)n(c2c1cccc2)C
EC Number:
233-714-8
NSC Number:
76087
Properties
Complexity:
251  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
177.043g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
177.159g/mol
Monoisotopic Mass:
177.043g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
46.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.9  
Literature
Title Journal
Identification and development of the 1,4-benzodiazepin-2-one and quinazoline-2,4-dione scaffolds as submicromolar inhibitors of HAT. Bioorganic & medicinal chemistry 20121015
Fingerprinting noncanonical and tertiary RNA structures by differential SHAPE reactivity. Journal of the American Chemical Society 20120815
Synthesis and characterization of a fluorescent analogue of cyclic di-GMP. Biochemistry 20120710
Automated RNA structure prediction uncovers a kink-turn linker in double glycine riboswitches. Journal of the American Chemical Society 20120125
Probing Retroviral and Retrotransposon Genome Structures: The 'SHAPE' of Things to Come. Molecular biology international 20120101
RNA folding and catalysis mediated by iron (II). PloS one 20120101
A universal pathway for kinesin stepping. Nature structural & molecular biology 20110901
Use of specific chemical reagents for detection of modified nucleotides in RNA. Journal of nucleic acids 20110101
1-Methyl-4H-3,1-benzoxazine-2,4(1H)dione. Acta crystallographica. Section E, Structure reports online 20100301
An upstream Hfq binding site in the fhlA mRNA leader region facilitates the OxyS-fhlA interaction. PloS one 20100101
A lanthanide-based chemosensor for bioavailable Fe3+ using a fluorescent siderophore: an assay displacement approach. Sensors (Basel, Switzerland) 20100101
Revisiting plus-strand DNA synthesis in retroviruses and long terminal repeat retrotransposons: dynamics of enzyme: substrate interactions. Viruses 20091201
SHAMS: combining chemical modification of RNA with mass spectrometry to examine polypurine tract-containing RNA/DNA hybrids. RNA (New York, N.Y.) 20090801
Influence of nucleotide identity on ribose 2'-hydroxyl reactivity in RNA. RNA (New York, N.Y.) 20090701
Ligand-dependent folding of the three-way junction in the purine riboswitch. RNA (New York, N.Y.) 20080401
High-throughput SHAPE analysis reveals structures in HIV-1 genomic RNA strongly conserved across distinct biological states. PLoS biology 20080401
Simultaneous determination of myo-inositol and scyllo-inositol by MEKC as a rapid monitoring tool for inositol levels. Electrophoresis 20070401
Microsphere-based protease assays and screening application for lethal factor and factor Xa. Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501
Selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE): quantitative RNA structure analysis at single nucleotide resolution. Nature protocols 20060101
RNA SHAPE chemistry reveals nonhierarchical interactions dominate equilibrium structural transitions in tRNA(Asp) transcripts. Journal of the American Chemical Society 20050406
RNA structure analysis at single nucleotide resolution by selective 2'-hydroxyl acylation and primer extension (SHAPE). Journal of the American Chemical Society 20050330
Are isatin and isatoic anhydride antiaromatic and aromatic respectively? A combined experimental and theoretical investigation. Organic & biomolecular chemistry 20030721
Properties