15934-46-0

Basic information

• Product Name: Benzamide, hydrochloride
• CAS NO: 15934-46-0
• Molecular Formula: C7H7NO.ClH
• Molecular Weight: 157.6
• Mol File: 15934-46-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzamide, hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, hydrochloride(15934-46-0)
• EPA Substance Registry System: Benzamide, hydrochloride(15934-46-0)

Safety Data

• Hazardous Substances Data: 15934-46-0(Hazardous Substances Data)

Upstream product

• 55-21-0 benzamide 
• 100-47-0 benzonitrile 
• 60199-37-3 N-benzoyl p-nitrobenzenesulfenamide 
• 81386-74-5 C₂₀H₁₅ClN₂O₂S 
• 7647-01-0 hydrogenchloride 
• 71151-37-6 p-chlorobenzene(N-benzoyl)iminosulfinyl chloride 
• 106-54-7 p-Chlorothiophenol 
• 70925-53-0 p-toluene(N-benzoyl)iminosulfinyl chloride 
• 106-45-6 para-thiocresol 
• 68556-47-8 N-benzoyl-p-chlorobenzenesulfenamide 
• 541-41-3 chloroformic acid ethyl ester 

Downstream Products

• 33643-94-6 2-phenyl-4-hydroxypyrimidine 
• 3749-46-0 2-phenyl-5-nitro-4-oxopyrimidine 
• 1266476-75-8 5-bromo-N-(5-cyclopropyl-2H-pyrazol-3-yl)-2-phenyl-pyrimidin-4-amine 
• 1266480-04-9 tert-butyl 5-cyclopropyl-3-(2-phenyl-5-((trimethylsilyl)ethynyl)pyrimidin-4-ylamino)-1H-pyrazole-1-carboxylate 
• 1266480-02-7 N-(5-cyclopropyl-1H-pyrazol-3-yl)-5-iodo-2-phenylpyrimidin-4-amine 
• 1266480-01-6 4-bromo-5-iodo-2-phenylpyrimidine 
• 1266480-00-5 5-iodo-2-phenylpyrimidin-4-ol 
• 26786-28-7 5-bromo-4-hydroxy-2-phenylpyrimidine 
• 1266477-07-9 (E)-N-(5-cyclopropyl-1H-pyrazol-3-yl)-5-(3-methoxyprop-1-enyl)-2-phenyl-pyrimidin-4-amine 
• 1266480-03-8 tert-butyl 5-cyclopropyl-3-(5-iodo-2-phenylpyrimidin-4-ylamino)-1H-pyrazole-1-carboxylate 
• 1266480-05-0 N-(5-cyclopropyl-1H-pyrazol-3-yl)-2-phenyl-5-((trimethylsilyl)ethynyl)pyrimidin-4-amine 
• 1266479-98-4 4,5-dibromo-2-phenylpyrimidine 
• 1266476-82-7 N-(5-cyclopropyl-1H-pyrazol-3-yl)-5-ethynyl-2-phenyl-pyrimidin-4-amine 
• 1227380-43-9 (S,S)-cyclohexenylimidazoline 

Relevant articles and documents

Efficient transformation of nitrile into amide under mild condition

Transformation of various kinds of nitriles into the corresponding amides or amide salts was performed in good yields by the addition of two equiv of chlorotrimethylsilane and two equiv of water at 0°C to 25°C.

Benzamide derivative analgesics

Benzamide derivative analgesic compounds of the formula STR1 wherein P, Q, R1, R2, X and Y are as defined in the specification, e.g., 3,4-Dichloro-N-[[8-(dimethylamino)-1,4-dioxaspiro[4.5]dec-8-yl]methyl]benzamide, and their pharmaco

OXIDATION IMINATION OF SULFENYL CHLORIDES BY N-CHLOROCARBOXAMIDES. N-ACYLSULFINIMIDOYL CHLORIDES

The reaction of arenesulfenyl chlorides ArSCl with N-chlorocarboxyamides in a ratio of 1:1 leads to the formation of N-acylsulfinimidoyl chlorides ArS(=NCOR)Cl.The reaction of arenesulfenyl chlorides and N-chlorobenzamide in ratio of 1:1 leads to aryldibenzamidosulfonium chlorides ArS(NHCOC6H5)2, which are hydrolyzed with the formation of N,N'-benzoylarenesulfinamidines ArS(=NCOC6H5)NHCOC6H5 and are cleaved into acid chlorides and benzamide when heated.