5843-46-9

Basic information

• Product Name: Benzoyl isocyanate, 4-methyl- (9CI)
• Synonyms: Benzoyl isocyanate, 4-methyl- (9CI)
• CAS NO: 5843-46-9
• Molecular Formula: C₉H₇NO₂
• Molecular Weight: 161.15738
• Product Categories: AMIDE
• Mol File: 5843-46-9.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzoyl isocyanate, 4-methyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl isocyanate, 4-methyl- (9CI)(5843-46-9)
• EPA Substance Registry System: Benzoyl isocyanate, 4-methyl- (9CI)(5843-46-9)

Safety Data

• Hazardous Substances Data: 5843-46-9(Hazardous Substances Data)

Upstream product

• 99-94-5 p-Toluic acid 
• 79-37-8 oxalyl dichloride 
• 917-61-3 sodium isocyanate 
• 874-60-2 4-methyl-benzoyl chloride 
• 619-55-6 para-methylbenzamide 
• 104825-41-4 1,1-Dimethyl-3,3-bis-(4-methyl-benzoyl)-urea 

Downstream Products

• 54201-24-0 N-(4-Methylbenzoyl)-peroxycarbamidsaeure-tert-butylester 
• 23252-23-5 3-ethyl-2-phenyl-6-p-tolyl-2,3-dihydro-[1,3,5]oxadiazin-4-one 
• 501433-84-7 1-[2-(2-methyl-aziridin-1-yl)-pyridin-3-yl]-3-(4-methyl-benzoyl)-urea 
• 1123689-75-7 C₁₉H₁₆N₄O₂S 
• 56800-16-9 N,N'-carbonylbis(4-methylbenzamide) 
• 1428619-92-4 2-[5-bromo-2-(4-methylbenzoylimino)benzo[d]thiazol-3(2H)-yl]butanoic acid 
• 1428619-95-7 methyl 2-[5-bromo-2-(4-methylbenzoylimino)benzo[d]thiazol-3(2H)-yl]butanoate 
• 1428619-94-6 N-(5-bromobenzo[d]thiazol-2-yl)-4-methylbenzamide 
• 1428619-93-5 N-(2,5-dibromophenylcarbamothioyl)-4-methylbenzamide 
• 1621584-41-5 N-(2-oxoindolin-6-ylcarbamoyl)-4-methylbenzamide 
• 66913-68-6 1-(N-4-methylbenzoyl-carbamoyl)-2-cyanoaziridine 
• 38354-35-7 5-p-tolyl-[1,2,4]dioxazol-3-one 
• 38354-40-4 5-morpholin-4-yl-5-p-tolyl-[1,2,4]dioxazolidin-3-one 
• 38336-45-7 (4-methyl-benzoyl)-peroxocarbamic acid 

Relevant articles and documents

Scalable Synthetic Strategy for Unsymmetrical Trisubstituted s-Triazines

A scalable synthetic strategy to produce a large variety of unsymmetrical trisubstituted 1,3,5-triazines was developed. This protocol applied in situ formed acyl isocyanate from amide to react with amidine, introducing two substituents to the 1,3,5-triazinone ring with a low production cost and a simple workup procedure. The scalability of this method was demonstrated by translating a small-scale procedure to a multi-kilogram-scale synthesis. Chlorination and a further coupling reaction with various nucleophiles could provide unsymmetrical trisubstituted 1,3,5-triazines bearing diverse functional groups.

A useful synthesis of 2-acylamino-1,3,4-oxadiazoles from acylthiosemicarbazides using potassium iodate and the discovery of new antibacterial compounds

A useful method for the synthesis of 2-acylamino-1,3,4-oxadiazoles was developed. By using potassium iodate as an oxidant in water at 60 ?C, a wide range of 2-acylamino-1,3,4-oxadiazoles were afforded in moderate to excellent yields within two

Design, synthesis and fungicidal activity of N-substituted benzoyl-1,2,3,4-tetrahydroquinolyl-1-carboxamide

To find a new lead compound with high biological activity, a series of N-substituted benzoyl-1,2,3,4-tetrahydroquinolyl-1-carboxamide were designed using linking active substructures method. The target compounds were synthesized from substituted benzoic acid by four steps and their structures were confirmed by 1H NMR, IR spectrum and elemental analysis. The in vitro bioassay results indicated that some target compounds exhibited excellent fungicidal activities, and the position of the substituents played an important role in fungicidal activities. Especially, compound 5n, exhibited better fungicidal activities than the commercial fungicide flutolanil against two tested fungi Valsa Mali and Sclerotinia sclerotiorum, with EC50 values of 3.44 and 2.63 mg/L, respectively. And it also displayed good in vivo fungicidal activity against S. sclerotiorum with the EC50 value of 29.52 mg/L.