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About This Item
Empirical Formula (Hill Notation):
C6H4N2O
CAS Number:
Molecular Weight:
120.11
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
form
solid
bp
75-85 °C/20 mmHg (lit.)
mp
47-51 °C (lit.)
SMILES string
c1ccc2nonc2c1
InChI
1S/C6H4N2O/c1-2-4-6-5(3-1)7-9-8-6/h1-4H
InChI key
AWBOSXFRPFZLOP-UHFFFAOYSA-N
Signal Word
Warning
Hazard Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
168.8 °F - closed cup
Flash Point(C)
76 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Tomofumi Santa et al.
Biomedical chromatography : BMC, 21(11), 1207-1213 (2007-06-26)
The applicability of benzofurazan derivatization regents to carboxylic acids analysis in LC/ESI-MS/MS (high-performance liquid chromatography/electrospray ionization tandem mass spectrometry) was examined. The product ion spectra of DAABD-AE {4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-(2-aminoethylamino)-2,1,3-benzoxadiazole}, DAABD-PZ {4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-N-piperazino-2,1,3-benzoxadiazole}, DAABD-PiCZ {4-[4-carbazoylpiperidin-1-yl]-7-[2-(N,N-dimethylamino)ethylaminosulfonyl]-2,1,3-benzoxadiazole}, DAABD-ProCZ {4-[2-carbazoylpyrrolidin-1-yl]-7-[2-(N,N-dimethylamino) ethylaminosulfonyl]-2,1,3-benzoxadiazole} and DAABD-Apy {4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole}, and their
Zhenghao Yang et al.
Dalton transactions (Cambridge, England : 2003), 40(10), 2173-2176 (2010-11-23)
Terpyridine/benzofurazan conjugation results in a new hybrid fluorophore of the colorimetric sensing ability for Fe(2+) and fluorimetric sensing ability for XII group cations. The improved emission properties and cell imaging ability imply it is a suitable platform to construct a
Zhipeng Liu et al.
The Journal of organic chemistry, 76(24), 10286-10290 (2011-11-18)
A dicyanovinyl-substituted benzofurazan derivative (C1) was prepared as an efficient ratiometric chemosensor for cyanide anion detection in aqueous acetonitrile solution. Mechanism studies suggested that the nucleophilic addition of cyanide to the α-position of the dicyanovinyl group blocked the ICT progress
Alex Brown et al.
The journal of physical chemistry. A, 116(1), 46-54 (2011-12-06)
General chemical strategies which provide controlled changes in the emission or absorption properties of biologically compatible fluorophores remain elusive. One strategy employed is the conversion of a fluorophore-attached alkyne (or azide) to a triazole through a copper-catalyzed azide-alkyne coupling (CuAAC)
Maki Onoda et al.
Chemical communications (Cambridge, England), (14)(14), 1848-1850 (2005-03-30)
Strong fluorescence signals were observed after the reaction of novel reagents with hydroperoxides.
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