61964-70-3

Basic information

• Product Name: Acetic acid, [[(2,4-dimethoxyphenyl)methyl]imino]-, methyl ester
• CAS NO: 61964-70-3
• Molecular Formula: C12H15NO4
• Molecular Weight: 237.255
• Mol File: 61964-70-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Acetic acid, [[(2,4-dimethoxyphenyl)methyl]imino]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, [[(2,4-dimethoxyphenyl)methyl]imino]-, methyl ester(61964-70-3)
• EPA Substance Registry System: Acetic acid, [[(2,4-dimethoxyphenyl)methyl]imino]-, methyl ester(61964-70-3)

Safety Data

• Hazardous Substances Data: 61964-70-3(Hazardous Substances Data)

Upstream product

• 922-68-9 Methyl glyoxylate 
• 20781-20-8 2,4-Dimethoxybenzylamine 

Downstream Products

• 613-45-6 2,4-Dimethoxybenzaldehyde 
• 83169-55-5 trans-3-benzyloxycarbonylamino-1-(2,4-dimethoxybenzyl)-4-methoxycarbonyl-2-azetidinone 
• 83169-55-5 cis-3-benzyloxycarbonylamino-1-(2,4-dimethoxybenzyl)-4-methoxycarbonyl-2-azetidinone 
• 61964-80-5 trans-1-(2,4-dimethoxybenzyl)-4-methoxycarbonyl-3-phthalimido-2-azetidinone 
• 61964-78-1 trans-3-amino-1-(2,4-dimethoxybenzyl)-4-methoxycarbonyl-2-azetidinone 
• 61964-78-1 cis-3-amino-1-(2,4-dimethoxybenzyl)-4-methoxycarbonyl-2-azetidinone 
• 92973-53-0 α-chloro-N-(2,4-dimethoxybenzyl)-N-phthalimidoacetylglycine 
• 92973-54-1 cis-3-benzyloxycarbonylamino-1-(2,4-dimethoxybenzoyl)-4-methoxycarbonyl-2-azetidinone 
• 91-52-1 2,4 dimethoxybenzoic acid 
• 92973-51-8 N-(2,4-dimethoxybenzyl)phthalimidoacetamide 
• 61964-80-5 cis-1-(2,4-dimethoxybenzyl)-4-methoxycarbonyl-3-phthalimido-2-azetidinone 
• 92973-52-9 methyl N-(2,4-dimethoxybenzyl)-N-(phthalimidoacetyl)immonioacetate chloride 
• 69177-79-3 Phthalimido-keten 

Relevant articles and documents

Chemical modification of sulfazecin. Synthesis of 4-methoxycarbonyl-2-azetidinone-1-sulfonic acid derivatives

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Methods and intermediates for preparing cis-4-oxoazetidine intermediates

The stereospecific cycloaddition of nitrogen containing acetic acid halides or anhydrides with Schiff bases having a carbalkoxy group substituted on the methine carbon atom offers new intermediates and methods for preparing synthetic cephalosporin congeners having antibacterial activity.

8-Oxo-4-thia-1-azabicyclo (4.2.0)-oct-2-ene derivatives

Novel bicyclic β-lactams and intermediates useful in their preparation are disclosed. In particular, 7β-acyl-amino- and 7β-amino-8-oxo-4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acids are prepared. The acylated compounds are antibacterial agents.