BENZANILIDE FOR SYNTHESIS

SKU: RXSOL-60-6604-038
Category: Lab Chemical-60
Supply Location: Locations [BENZANILIDE FOR SYNTHESIS] manufacturers, suppliers, exporters in Mumbai, Gandhidham, Kolkata, Varanasi, Visakhapatnam, Chennai, Fujairah, Dubai, Canada BC, Barka, Sohar, Muscat, Oman. Lab   chemicals manufacturers, suppliers, exporters in India, UAE Middle East, Barka, Sohar, Muscat, Oman, Canada.   [BENZANILIDE FOR SYNTHESIS] is available in small packing as well as in bulk. Buy premium quality [BENZANILIDE FOR SYNTHESIS] and other lab chemicals from one of the most trusted brands.

Benzanilide is the organic compound with the formula C6H5C(O)NHC6H5. It is a white solid. Commercially available, it may be prepared by treating benzoic acid with aniline.

Benzanilide synthesis through amide bond formation was effectively carried out by palladium-doped clay catalyst using microwave irradiation under solvent-free conditions. Products were obtained with excellent yield in very short reaction time and only a small amount of the catalyst was used.



The ordinary "pure" aniline of commerce gives as good yields and as pure a product as redistilled aniline. The benzanilide must be finely ground in order that aniline and benzoic acid may be completely extracted.

Information on basic physical and chemical properties
Odour threshold :                                                                              No data available
pH :                                                                                                   No data available
Relative evaporation rate (butylacetate=1) :                                     No data available
Melting point :                                                                                           161 - 163 °C
Freezing point :                                                                                 No data available
Boiling point :                                                                                                     117 °C
Flash point :                                                                                      No data available
Auto-ignition temperature :                                                                No data available
Decomposition temperature :                                                            No data available
Flammability (solid, gas) :                                                                 No data available
Vapour pressure :                                                                              No data available
Relative vapour density at 20 °C :                                                     No data available
Relative density :                                                                               No data available
Density :                                                                                                     1.315 g/cm³
Solubility : Water:                                                                               Insoluble in water
Log Pow :                                                                                          No data available
Viscosity, kinematic :                                                                         No data available
Viscosity, dynamic :                                                                           No data available
Explosive properties :                                                                       No data available
Oxidising properties :                                                                        No data available
Explosive limits :                                                                               No data available
Benzanilide undergoes diarylation with aryl triflates or bromides in the presence of a palladium-based catalyst system to form corresponding N-(2,6-diarylbenzoyl)anilines. It is used in manufacture of dyes and perfumes.

Insertion of benzoyl moiety instead of an active hydrogen atom present in hydroxyl (OH) primary amino (NH2) or secondary amino group (NH) is usually termed as benzoylation reaction. 


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