ChemicalBook >> CAS DataBase List >>p-Nitrobenzamide

p-Nitrobenzamide

CAS No.
619-80-7
Chemical Name:
p-Nitrobenzamide
Synonyms
NitrobenzaMide;P-NITROBENZAMIDE;p-nitro-benzamid;4-NITROBENZAMIDE;4-nitro-benzamid;Benzamide,4-nitro-;Benzamide,p-nitro-;TIMTEC-BB SBB008201;Benzamide, p-nitro-;4-Nitrobenzamide>
CBNumber:
CB5369841
Molecular Formula:
C7H6N2O3
Molecular Weight:
166.13
MDL Number:
MFCD00007994
MOL File:
619-80-7.mol
MSDS File:
SDS
Last updated:2023-04-23 13:52:06

p-Nitrobenzamide Properties

Melting point 199-201 °C(lit.)
Boiling point 294.32°C (rough estimate)
Density 1.4334 (rough estimate)
refractive index 1.5880 (estimate)
pka 15.02±0.50(Predicted)
form powder to crystal
color White to Orange to Green
Water Solubility <0.01 g/100 mL at 18 ºC
BRN 639263
Stability Stable. Incompatible with strong oxidizing agents, strong bases.
CAS DataBase Reference 619-80-7(CAS DataBase Reference)
EWG's Food Scores 1
NIST Chemistry Reference Benzamide, 4-nitro-(619-80-7)
EPA Substance Registry System p-Nitrobenzamide (619-80-7)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P301+P312+P330
Hazard Codes  T,Xn
Risk Statements  23/24/25-22-20/21/22
Safety Statements  27-28-36/37/39-45-36
WGK Germany  3
RTECS  CV5601000
TSCA  Yes
HS Code  29242990
NFPA 704
1
2 0

p-Nitrobenzamide Chemical Properties,Uses,Production

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

General Description

White powder.

Air & Water Reactions

Insoluble in water.

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).

Fire Hazard

Flash point data for p-Nitrobenzamide are not available, however, p-Nitrobenzamide is probably combustible.

p-Nitrobenzamide Preparation Products And Raw materials

Raw materials

Preparation Products

p-nitro-benzamid P-NITROBENZAMIDE TIMTEC-BB SBB008201 4-Nitrobenzamide p-Nitrobenzamide 4-Nitrobenzamide>99.0% 4-NITROBENZAMIDE 4-Nitrobenzamide, 98+% 4-Carbamoylnitrobenzene ForMaMide nitrobenzene NitrobenzaMide 4-nitro benzoylaMide The nitrobenzene forMaMide 4-nitro-benzamid 4-Nitrobenzoesαureamid 4-Nitrobenzoicacid,amide Benzamide, p-nitro- Benzamide,4-nitro- Benzamide,p-nitro- 4-Nitrobenzamide (>=99%) 4-Nitrobenzamide> 619-80-7 O2NC6H4CONH2 NO2C6H4CONH2 Organic Building Blocks Carbonyl Compounds Amides Building Blocks Pharmaceutical Intermediates Amides Carbonyl Compounds Organic Building Blocks Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts