55985-04-1

Basic information

• Product Name: methyl (S)-4-methylsulfanyl-2-phthalimidobutanoate
• Synonyms: methyl (S)-4-methylsulfanyl-2-phthalimidobutanoate
• CAS NO: 55985-04-1
• Molecular Weight: 293.343
• Mol File: 55985-04-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl (S)-4-methylsulfanyl-2-phthalimidobutanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (S)-4-methylsulfanyl-2-phthalimidobutanoate(55985-04-1)
• EPA Substance Registry System: methyl (S)-4-methylsulfanyl-2-phthalimidobutanoate(55985-04-1)

Safety Data

• Hazardous Substances Data: 55985-04-1(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 74242-84-5 C₁₃H₁₂ClNO₃S 
• 5464-44-8 1,3-dihydro-1,3-dioxo-α(CH2CH2SCH3)-2H-isoindole-2-acetate 
• 85-44-9 phthalic anhydride 
• 59-51-8 DL-methionine 
• 10332-17-9 Met-OMe 

Downstream Products

• 109541-75-5 methyl 1-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)cyclopropanecarboxylate 

Relevant articles and documents

Stereoselective synthesis of functional derivatives of 2-(2-carboxyethyl) pyrrolidine-2-carboxylic acid

Azomethine ylides generated from dimethyl 2-(arylmethylideneamino) pentanedioates by the action of AgOAc and Et3N reacted with dipolarophiles in regio- and stereoselective fashion to form 5-aryl-2-(2-carboxyethyl)pyrrolidine-2-carboxylic acid derivatives. 1,3-Dipolar cycloaddition of divinyl sulfone to the azomethine ylide generated from the Schiff base derived from methyl (S)-2-phthalimido-4-oxobutanoate and dimethyl glutamate gave chiral simplified kaitocephalin analogs. Pleiades Publishing, Inc., 2006.