69053-95-8

Basic information

• Product Name: Benzoic acid, 2-[chloro(hydroxyimino)methyl]-, methyl ester
• CAS NO: 69053-95-8
• Molecular Formula: C9H8ClNO3
• Molecular Weight: 213.62
• Mol File: 69053-95-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-[chloro(hydroxyimino)methyl]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-[chloro(hydroxyimino)methyl]-, methyl ester(69053-95-8)
• EPA Substance Registry System: Benzoic acid, 2-[chloro(hydroxyimino)methyl]-, methyl ester(69053-95-8)

Safety Data

• Hazardous Substances Data: 69053-95-8(Hazardous Substances Data)

Upstream product

• 4122-56-9 methyl o-formylbenzoate 
• 69053-94-7 Methyl 2-(hydroximinomethyl)benzoate 

Downstream Products

• 69958-02-7 Methyl 2-<5-(2-pyridyl)-1,2,4-oxadiazol-3-yl>benzoate 
• 70001-64-8 Methyl 2-<5-(4-chlorophenyl)-2-isoxazolin-3-yl>benzoate 
• 70001-68-2 Methyl 2-<5-(3,4-methylenedioxyphenyl)-2-isoxazolin-3-yl>benzoate 
• 69958-01-6 Methyl 2-<5-(3-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl>benzoate 
• 69958-03-8 Methyl 2-(5-phenyl-1,2,4-oxadiazol-3-yl)benzoate 
• 83727-34-8 3,4-Bis(2-methoxycarbonylphenyl)furazan oxide 
• 69958-00-5 Methyl 2-<5-(4-methoxyphenyl)-1,2,4-oxadiazol-3-yl>benzoate 
• 164254-44-8 2-(5-Phenyl-4,5-dihydro-isoxazol-3-yl)-benzoic acid methyl ester 
• 83727-29-1 Methyl 2-<5-<3-(trifluoromethyl)phenyl>isoxazol-3-yl>benzoate 

Relevant articles and documents

Iron Promoted Ring Opening and Ring Closing Cascade (ROCC) Reaction of Ortho-Carboxy-Isoxazoles Leading to Isoindolinone Derivatives

An efficient and convenient route for the synthesis of various functionalized 3-alkylidene isoindolin-1-ones is presented. The synthesis involves the ring opening and ring closing cascade (ROCC) reaction of ortho-carboxy-isoxazole using Fe/NH4Cl. This is the first report for the synthesis of 3-alkylidene isoindolin-1-one using Fe/NH4Cl.

NOVEL N-[(PYRAZINYLOXY)PROPANYL]BENZAMIDES

This invention relates to compounds of formula (I) a process for their preparation, pharmaceutical compositions containing them and their use in the treatment of conditions having an association with the orexin sub-type 1 receptor. Ar, R1, Rsu

Nitrile Oxide Cycloaddtion Routes to 2-(Isoxazolyl)benzoates and 2-(1,2,4-Oxadiazol-3-yl)benzoates

Cycloaddition of aromatic nitrile oxides to methyl o-vinylbenzoate produced methyl 2-(3-aryl-2-isoxazolin-5-yl)benzoates; the isoxazolines were converted to methyl 2-(3-arylisoxazol-5-yl)benzoates.Reaction of the nitrile oxide from o-methoxycarbonylbenzohydroximinoyl chloride (11) with phenylacetylene, styrenes, and aromatic nitriles resulted in methyl 2-(5-phenylisoxazol-3-yl)benzoate, methyl 2-(5-aryl-2-isoxazolin-3-yl)benzoates (15) and methyl 2-(5-aryl-1,2,4-oxadiazol-3-yl)benzoates, respectively.The isoxazolines 15 were converted to the corresponding isoxazoles 16.