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610-15-1

610-15-1 Structure

610-15-1 Structure
IdentificationMore
[Name]

2-NITROBENZAMIDE
[CAS]

610-15-1
[Synonyms]

2-NITROBENZAMIDE
O-NITROBENZAMIDE
TIMTEC-BB SBB008239
2-Carbamoylnitrobenzene
2-nitro-benzamid
2-Nitrobenzoesαureamid
Benzamide, o-nitro-
Benzamide,2-nitro-
Benzmide, 2-nitro-
o-nitro-benzamid
2-Nitrobenzamide,98%
[EINECS(EC#)]

210-208-5
[Molecular Formula]

C7H6N2O3
[MDL Number]

MFCD00007976
[Molecular Weight]

166.13
[MOL File]

610-15-1.mol
Chemical PropertiesBack Directory
[Appearance]

beige crystalline powder
[Melting point ]

174-178 °C (lit.)
[Boiling point ]

317 °C (lit.)
[density ]

1.384
[refractive index ]

1.5880 (estimate)
[Fp ]

317°C
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

15.09±0.50(Predicted)
[BRN ]

1950928
[CAS DataBase Reference]

610-15-1(CAS DataBase Reference)
[EPA Substance Registry System]

o-Nitrobenzamide (610-15-1)
Safety DataBack Directory
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[RTECS ]

CV5600000
[HS Code ]

29242998
Hazard InformationBack Directory
[General Description]

Water solubility-<0.1 mg/mL at 64°F.
[Reactivity Profile]

A nitrated amide. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).
[Air & Water Reactions]

Insoluble in water.
[Fire Hazard]

Flash point data for this chemical are not available, however O-NITROBENZAMIDE is probably combustible.
[Chemical Properties]

beige crystalline powder
[Uses]

2-Nitrobenzamide was used in the synthesis of novel fluorogenic chemosensors based on urea derivative of 2-(2′-aminophenyl)-4-phenylthiazole. It was also used in the synthesis of quinazoline-2,4(1H,3H)-diones, an important class of pharmaceutical intermediates.
Spectrum DetailBack Directory
[Spectrum Detail]

2-NITROBENZAMIDE(610-15-1)MS
2-NITROBENZAMIDE(610-15-1)1HNMR
2-NITROBENZAMIDE(610-15-1)13CNMR
2-NITROBENZAMIDE(610-15-1)IR1
2-NITROBENZAMIDE(610-15-1)IR2
2-NITROBENZAMIDE(610-15-1)IR3
2-NITROBENZAMIDE(610-15-1)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2-Nitrobenzamide, 98%(610-15-1)
[Alfa Aesar]

2-Nitrobenzamide, 98%(610-15-1)
[Sigma Aldrich]

610-15-1(sigmaaldrich)
[TCI AMERICA]

2-Nitrobenzamide,>98.0%(T)(610-15-1)
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