937737-95-6

Basic information

• Product Name: thioacetic acid S-(4-tert-butoxycarbonylaminophenyl) ester
• Synonyms: thioacetic acid S-(4-tert-butoxycarbonylaminophenyl) ester
• CAS NO: 937737-95-6
• Molecular Weight: 267.349
• Mol File: 937737-95-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: thioacetic acid S-(4-tert-butoxycarbonylaminophenyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: thioacetic acid S-(4-tert-butoxycarbonylaminophenyl) ester(937737-95-6)
• EPA Substance Registry System: thioacetic acid S-(4-tert-butoxycarbonylaminophenyl) ester(937737-95-6)

Safety Data

• Hazardous Substances Data: 937737-95-6(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 131818-17-2 tert-butyl (4-bromophenyl)carbamate 
• 10387-40-3 potassium thioacetate 
• 722-27-0 bis(4-aminophenyl)disulfide 
• 1193-02-8 4-aminotiophenol 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 42467-06-1 p-Aminophenylthiol-acetat 

Relevant articles and documents

A helical molecule that exhibits two lengths in response to an applied potential

(Figure Presented) Outstanding in the electric field: Bundles of helical peptides undergo stochastic switching in response to the applied bias polarity as observed by STM. This behavior results from a conformational change between the α-helical (left) and

Efficient preparation of S-aryl thioacetates from aryl halides and potassium thioacetate

A method for the preparation of S-aryl thioacetates using palladium-mediated couplings of aryl bromides and aryl triflates with potassium thioacetate as an inexpensive thiol source was developed. Electron withdrawing groups, electron donating groups and heterocyclic substrates were tolerated in the reaction conditions, affording the corresponding products in good to excellent yields. This method was applied to the preparation of novel sulfone-containing DPP-IV inhibitors.