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

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

Downstream Products

• 331821-49-9 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 
• 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 
• 331821-52-4 (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 

Relevant articles and documents

DENTRITIC POLYMERS, CROSSLINKED GELS, AND THEIR USES IN ORTHOPEDIC APPLICATIONS

The present invention provides compositions, kits, and methods for repairing cartilaginous tissue. Certain methods of the invention utilize dendritic macromolecules formed by treating a dendritic compound with light or a linking compound. In certain instances, the dendritic compounds have a lysine, cysteine, isocysteine residue or other nucleophilic group attached to their peripheries. Addition of a compound containing two or more electrophilic groups, such as aldehydes, activated esters, or acrylates, to the lysine-capped, cysteine-capped, or isocysteine-capped dendrimers produces a polymeric compound that can repair a cartilage defect.

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