17335-06-7

Basic information

• Product Name: 4-Benzoyl-5-methyl-3-isoxazolecarboxylic acid ethyl ester
• Synonyms: 4-Benzoyl-5-methyl-3-isoxazolecarboxylic acid ethyl ester
• CAS NO: 17335-06-7
• Molecular Formula: C₁₄H₁₃NO₄
• Molecular Weight: 259.2573
• Mol File: 17335-06-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 373.2°Cat760mmHg
• Flash Point: 179.5°C
• Appearance: /
• Density: 1.21g/cm³
• Vapor Pressure: 9.14E-06mmHg at 25°C
• Refractive Index: 1.544
• CAS DataBase Reference: 4-Benzoyl-5-methyl-3-isoxazolecarboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Benzoyl-5-methyl-3-isoxazolecarboxylic acid ethyl ester(17335-06-7)
• EPA Substance Registry System: 4-Benzoyl-5-methyl-3-isoxazolecarboxylic acid ethyl ester(17335-06-7)

Safety Data

• Hazardous Substances Data: 17335-06-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H13NO4/c1-3-18-14(17)12-11(9(2)19-15-12)13(16)10-7-5-4-6-8-10/h4-8H,3H2,1-2H3

Upstream product

• 95080-93-6 ethyl chlorooximidoacetate 
• 6710-62-9 1-phenyl-2-butyn-1-one 
• 626-35-7 nitroacetic acid ethyl ester 
• 93-91-4 1-phenylbutan-1,3-dione 
• 861135-87-7 chlorohydroxyimino-acetic acid ethyl ester 

Downstream Products

• 19688-11-0 4-benzoyl-5-styryl-isoxazole-3-carboxylic acid 
• 19925-77-0 4-benzoyl-5-methyl-isoxazole-3-carboxylic acid anilide 
• 19925-78-1 4-benzoyl-5-methyl-isoxazole-3-carboxylic acid diethylamide 
• 19925-75-8 4-benzoyl-5-methyl-isoxazole-3-carbonyl chloride 
• 25506-01-8 3-methyl-4,6-diphenyl-6H-isoxazolo[3,4-d]pyridazin-7-one 
• 121910-76-7 5-Acetyl-2-cyclohexyl-4-nitro-6-phenyl-2H-pyridazin-3-one 
• 17335-08-9 5-acetyl-4-aminopyridazinone 
• 121910-72-3 6-Cyclohexyl-3-methyl-4-phenyl-6H-isoxazolo[3,4-d]pyridazin-7-one 
• 108311-83-7 5-acetyl-4-amino-2-methyl-6-phenylpyridazin-3-(2H)-one 
• 17334-68-8 3-methyl-4-phenylisoxazolo[3,4-d]pyridazin-7(6H)-one 
• 19925-73-6 4-benzoyl-5-methyl-isoxazole-3-carboxylic acid 
• 19925-76-9 4-benzoyl-5-methyl-isoxazole-3-carboxylic acid amide 
• 51244-56-5 6-(2-diethylamino-ethyl)-3-methyl-4-phenyl-6H-isoxazolo[3,4-d]pyridazin-7-one 
• 51244-55-4 6-(2-dimethylamino-ethyl)-3-methyl-4-phenyl-6H-isoxazolo[3,4-d]pyridazin-7-one 

Relevant articles and documents

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Primary nitro compounds have not been employed as nitrile oxide precursors in reactions with active methylene compounds because the reagents commonly used as dehydrating agents also react with these dipolarophiles. However, the Cu II-catalysed

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