781-94-2

Basic information

• Product Name: 5-(Trifluoromethyl)isatoic anhydride
• Synonyms: 5-(Trifluoromethyl)isatoic anhydride;6-Trifluoromethyl-1H-benzo[d][1,3]oxazine-2,4-dione
• CAS NO: 781-94-2
• Molecular Formula: C₉H₄F₃NO₃
• Molecular Weight: 231.1281696
• Mol File: 781-94-2.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-(Trifluoromethyl)isatoic anhydride(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(Trifluoromethyl)isatoic anhydride(781-94-2)
• EPA Substance Registry System: 5-(Trifluoromethyl)isatoic anhydride(781-94-2)

Safety Data

• Hazardous Substances Data: 781-94-2(Hazardous Substances Data)

Upstream product

• 124-38-9 carbon dioxide 
• 201230-82-2 carbon monoxide 
• 163444-17-5 2-iodo-4-(trifluoromethyl)aniline 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 83265-53-6 2-amino-5-(trifluoromethyl)benzoic acid 
• 141940-29-6 2-(tert-butoxycarbonylamino)-5-(trifluoromethyl)benzoic acid 

Downstream Products

• 1361967-11-4 C₂₃H₁₄F₆N₂O₂ 
• 1433904-27-8 2-cyclopentyl-4-hydroxy-6-trifluoromethyl-quinoline-3-carbonitrile 
• 16499-54-0 2-amino-5-(trifluoromethyl)benzamide 
• 1361004-85-4 C₂₅H₁₇F₆NO₂ 
• 1361005-79-9 2-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)-4-(trifluoromethyl)aniline 
• 144155-44-2 1-[(E)-3-Dimethylamino-propylimino]-7-trifluoromethyl-3-(4-trifluoromethyl-phenyl)-1,3,4,10-tetrahydro-2H-acridin-9-one 
• 144155-14-6 7-Trifluoromethyl-3-(4-trifluoromethyl-phenyl)-3,4-dihydro-2H,10H-acridine-1,9-dione 

Relevant articles and documents

FUSED HETEROCYCLIC COMPOUNDS AND THEIR USE AS PEST CONTROL AGENTS

The present invention discloses a fused heterocyclic compound of formula (I) wherein, R1, G1, G2, G3, G4, A1, A2, Q, n and Z are as defined in the detailed description. The prese

Identification of a Novel 1,2,3,4-Tetrahydrobenzo[b][1,6]naphthyridine Analogue as a Potent Phosphodiesterase 5 Inhibitor with Improved Aqueous Solubility for the Treatment of Alzheimer's Disease

Phosphodiesterase 5 (PDE5) hydrolyzes cyclic guanosine monophosphate (cGMP) leading to increased levels of the cAMP response element binding protein (CREB), a transcriptional factor involved with learning and memory processes. We previously reported poten

Synthesis and Nematicidal Activities of 1,2,3-Benzotriazin-4-one Derivatives against Meloidogyne incognita

A series of novel 1,2,3-benzotriazin-4-one derivatives were synthesized by the reaction of 3-bromoalkyl-1,2,3-benzotriazin-4-ones with potassium salt of 2-cyanoimino-4-oxothiazolidine in the presence of potassium iodide. Nematicidal assays in vivo showed that some of them exhibited good control efficacy against the cucumber root-knot nematode disease caused by Meloidogyne incognita, up to 100% at the concentration of 10.0 mg L-1, which indicated that 1,2,3-benzotriazin-4-one derivatives might be potential for novel promising nematicides. The nematicidal activity was influenced by the combination of substituent type, substituted position, and linker length in the molecule. The inhibition rate data at the concentrations of 5.0 and 1.0 mg L-1 for the compounds with high inhibitory activities were also provided. When tested in vitro, none of them showed direct inhibition against M. incognita. The investigation of a significant difference between in vivo and in vitro data is in progress.