115934-14-0

Basic information

• Product Name: 2-{[(benzoylamino)carbothioyl]amino}benzamide
• Synonyms: 2-{[(benzoylamino)carbothioyl]amino}benzamide;2-{[(benzoylamino)carbonothioyl]amino}benzamide
• CAS NO: 115934-14-0
• Molecular Formula: C₁₅H₁₃N₃O₂S
• Molecular Weight: 299.34762
• Mol File: 115934-14-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-{[(benzoylamino)carbothioyl]amino}benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{[(benzoylamino)carbothioyl]amino}benzamide(115934-14-0)
• EPA Substance Registry System: 2-{[(benzoylamino)carbothioyl]amino}benzamide(115934-14-0)

Safety Data

• Hazardous Substances Data: 115934-14-0(Hazardous Substances Data)

Upstream product

• 1147550-11-5 ammonium thiocyanate 
• 98-88-4 benzoyl chloride 
• 28144-70-9 anthranilic acid amide 
• 532-55-8 Benzoyl isothiocyanate 

Downstream Products

• 1022-45-3 2-phenyl-4(3H)-quinazolinone 
• 131357-77-2 N-(4-oxo-4H-benzo[d][1,3]thiazin-2-yl)benzamide 
• 13906-09-7 2-thioxo-2,3-dihydro-1H-quinazolin-4-one 

Relevant articles and documents

A facile one-pot synthesis of substituted N-{[2-(aminocarbonyl)phenylamino]thioxomethyl}benzamides and 2-aryl-quinazolin-4(3H)-ones

The substituted N-{[2-(aminocarbonyl)phenylamino]thioxomethyl}benzamides and 2-arylquinazolin-4(3H)-ones are synthesized by the reaction of ammonium thiocyanate and aroyl chlorides with 2-amino-benzamide under solvent-free conditions or under reflux in MeCN.

Substituted N-[[2-(aminocarbonyl)phenylamino]thioxomethyl]benzamides

New substituted N-[[2-(aminocarbonyl)phenylamino]-thioxomethyl]benzamides which are useful as congnition stimulators in mammals.

A FACILE PREPARATION OF 3-SUBSTITUTED 2-THIOXO-TETRAHYDROQUINAZOLIN-4-ONES BY THE REACTION OF ANTHRANILAMIDE WITH ISOTHIOCYANATES

3-Substituted 2-thioxo-tetrahydroquinazolin-4-ones (4a-d) can be synthesized in a convenient procedure directly by a treatment of anthranilamide with isothiocyanates at room temperature.However, anthranilamide was reacted with 4-isothiocyanato-1-benzylpiperidine (2e) leading to the formation of 2-thioureidobenzamide (3e) which was subsequently cyclized to 4e under a basic condition.