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

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

Downstream Products

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

Relevant articles and documents

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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.

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CHEMISTRY OF IMINOSULFINIC ACIDS. REACTION OF N-ACYLIMINOSULFINYL CHLORIDES WITH THIOPHENOLS

Arene(N-benzoyl)- and arene(N-phenylsulfonyl)iminosulfinyl chlorides on reaction with thiophenols are reduced to N-(benzoyl) or N-(phenylsulfonyl)arenesulfenamides.When N-benzoyliminosulfinyl chlorides are reacted with thiophenols in the presence of triethylamine, a mixture of diaryl sulfides, NN-di(arylthio)benzamide, and N-arylthio-NN'-dibenzoylarenesulfinamidines is obtained.On heating, the latter reversibly dissociate to stable N-arylthio-N-benzoylaminyl radicals.