57892-27-0

Basic information

• Product Name: Benzoic acid, 2-nitroso-, ethyl ester
• CAS NO: 57892-27-0
• Molecular Formula: C9H9NO3
• Molecular Weight: 179.175
• Mol File: 57892-27-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-nitroso-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-nitroso-, ethyl ester(57892-27-0)
• EPA Substance Registry System: Benzoic acid, 2-nitroso-, ethyl ester(57892-27-0)

Safety Data

• Hazardous Substances Data: 57892-27-0(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 610-34-4 ethyl 2-nitrobenzoate 
• 38476-40-3 ethyl 2-(hydroxyamino)benzoate 
• 87-25-2 2-ethoxycarbonylaniline 
• 75-03-6 ethyl iodide 
• 552-89-6 2-nitro-benzaldehyde 
• 88356-11-0 o-nitrobenzaldehyde diethylacetal 

Downstream Products

• 57892-31-6 2-(5-oxo-3,4-diphenyl-5H-isoxazol-2-yl)-benzoic acid ethyl ester 
• 93-89-0 benzoic acid ethyl ester 
• 1579998-93-8 (E)-ethyl 2-((2-aminophenyl)diazenyl)benzoate 
• 15037-78-2 N-(2-Carboxyphenyl)-N'-p-toluolsulfonyldiimid-N-oxid 
• 15037-76-0 N-(2-Carboxyphenyl)-N'-fluordiimid-N-oxid 
• 573-79-5 2,2'-azoxy-di-benzoic acid 
• 15037-80-6 N-(2-Carbethoxyphenyl)-N'-fluordiimid-N-oxid 
• 15037-81-7 N-(2-Carbethoxyphenyl)-N'-p-toluolsulfonyldiimid-N-oxid 

Relevant articles and documents

Azobenzene-benzoylphenylureas as photoswitchable chitin synthesis inhibitors

Benzoylphenylureas (BPUs) are used as synthetic insect growth regulators for inhibiting chitin synthesis. Merging insecticidal BPUs with photoswitchable azobenzene generated photoresponsive chitin synthesis inhibitors. A prepared azobenzene-benzoylphenylurea can be activated upon irradiation with UV light, and shows 6-fold and 2-fold activity difference to armyworm (Mythimna separata) and German cockroach (Blattella germanica) sulfonylurea receptors, respectively. This is the first example of a photoswitchable BPU insecticide. The generation of such a photoresponsive BPU insecticide allows for modulation of the insecticidal activity by light, and may facilitate the spatiotemporal control over the sulfonylurea receptor and the mechanistic study of this kind of insecticide.