Identification | More | [Name]
p-Nitrobenzamide | [CAS]
619-80-7 | [Synonyms]
4-NITROBENZAMIDE P-NITROBENZAMIDE TIMTEC-BB SBB008201 4-nitro-benzamid 4-Nitrobenzoesαureamid 4-Nitrobenzoicacid,amide Benzamide, p-nitro- Benzamide,4-nitro- Benzamide,p-nitro- p-nitro-benzamid 4-Nitrobenzamide p-Nitrobenzamide 4-Nitrobenzamide>99.0% 4-Nitrobenzamide, 98+% | [EINECS(EC#)]
210-613-7 | [Molecular Formula]
C7H6N2O3 | [MDL Number]
MFCD00007994 | [Molecular Weight]
166.13 | [MOL File]
619-80-7.mol |
Safety Data | Back Directory | [Hazard Codes ]
T,Xn | [Risk Statements ]
R23/24/25:Toxic by inhalation, in contact with skin and if swallowed . R22:Harmful if swallowed. R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S27:Take off immediately all contaminated clothing . S28:After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer) . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [RTECS ]
CV5601000
| [TSCA ]
Yes | [HS Code ]
29242990 |
Hazard Information | Back Directory | [General Description]
White powder. | [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 compound are not available, however, P-NITROBENZAMIDE is probably combustible. | [Chemical Properties]
white powder | [Uses]
4-Nitrobenzamide was used in the preparation of 4-nitrobenziminosulfurane. | [Synthesis Reference(s)]
Tetrahedron Letters, 36, p. 3469, 1995 DOI: 10.1016/0040-4039(95)00528-K |
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