120711-54-8

Basic information

• Product Name: L-(-)-N-(tert-butyloxycarbonyl)-2,2-dimethylthiazolidinecarboxylic acid pentafluorophenyl ester
• Synonyms: L-(-)-N-(tert-butyloxycarbonyl)-2,2-dimethylthiazolidinecarboxylic acid pentafluorophenyl ester
• CAS NO: 120711-54-8
• Molecular Weight: 427.392
• Mol File: 120711-54-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: L-(-)-N-(tert-butyloxycarbonyl)-2,2-dimethylthiazolidinecarboxylic acid pentafluorophenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-(-)-N-(tert-butyloxycarbonyl)-2,2-dimethylthiazolidinecarboxylic acid pentafluorophenyl ester(120711-54-8)
• EPA Substance Registry System: L-(-)-N-(tert-butyloxycarbonyl)-2,2-dimethylthiazolidinecarboxylic acid pentafluorophenyl ester(120711-54-8)

Safety Data

• Hazardous Substances Data: 120711-54-8(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 67089-92-3 L-(-)-2,2-dimethylthiazolidine-4-carboxylic acid hydrochloride salt 
• 5317-15-7 (4R)-3-(tert-butoxycarbonyl)-2,2-dimethylthiazolidine-4-carboxylic acid 
• 771-61-9 2,3,4,5,6-pentafluorophenol 

Downstream Products

• 331821-52-4 (R)-4-[(S)-1-((2S,4R)-4-Benzyl-5-oxo-tetrahydro-furan-2-yl)-propylcarbamoyl]-2,2-dimethyl-thiazolidine-3-carboxylic acid tert-butyl ester 
• 331821-26-2 (R)-4-((S)-1-{(R)-Hydroxy-[(1R,2R,3S)-2-((S)-1-methoxycarbonyl-3-methylsulfanyl-propylcarbamoyl)-3-phenyl-cyclopropyl]-methyl}-propylcarbamoyl)-2,2-dimethyl-thiazolidine-3-carboxylic acid tert-butyl ester 
• 331821-49-9 N-Boc-L-2,2-dimethylthiazolidine-4-carbonyl-L-ethylglycyl-L-phenylalanyl-L-methionine methyl ester 
• 917252-86-9 R-2,2-dimethyl-3-(1,1-dimethylethoxycarbonyl)-N-(2-(4-nitrophenyl)ethyl)tetrahydrothiazole-4-carboxamide 

Relevant articles and documents

Effects of steric bulk and stereochemistry on the rates of?diketopiperazine formation from N-aminoacyl-2,2-dimethylthiazolidine-4-carboxamides (Dmt dipeptide amides)-a model for a new prodrug linker system

A peptide-like self-immolative molecular clip is required for release of active drugs from prodrugs by endopeptidases. Upon cleavage from the carrier, this clip must collapse and release the drug rapidly. A series of aminoacyl-5,5-dimethylthiaproline (Aaa

Dendritic macromers as in situ polymerizing biomaterials for securing cataract incisions

Dendritic macromers are attractive macromolecules for hydrogel formation since high cross-linking densities at low polymer concentration can be obtained, varied physical properties can be observed based on the macromer structure, and low viscous aqueous s