924627-62-3

Basic information

• Product Name: tert-butyl 2-bromo-4-(trifluoromethyl)phenylcarbamate
• Synonyms: tert-butyl 2-bromo-4-(trifluoromethyl)phenylcarbamate
• CAS NO: 924627-62-3
• Molecular Formula: C₁₂H₁₃BrF₃NO₂
• Molecular Weight: 340
• Mol File: 924627-62-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: tert-butyl 2-bromo-4-(trifluoromethyl)phenylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 2-bromo-4-(trifluoromethyl)phenylcarbamate(924627-62-3)
• EPA Substance Registry System: tert-butyl 2-bromo-4-(trifluoromethyl)phenylcarbamate(924627-62-3)

Safety Data

• Hazardous Substances Data: 924627-62-3(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 57946-63-1 4-amino-3-bromobenzotrifluoride 
• 141940-37-6 tert-butyl (4-(trifluoromethyl)phenyl)carbamate 

Downstream Products

• 220107-42-6 tert-butyl N-[2-methyl-4-(trifluoromethyl)phenyl]carbamate 
• 1370735-33-3 tert-butyl 2-bromo-4-(trifluoromethyl)phenyl(((chloromethyl)dimethylsilyl)methyl)carbamate 
• 1057720-52-1 tert-butyl N-[2-bromo-4-(trifluoromethyl)phenyl]-N-(prop-2-ynyl)carbamate 

Relevant articles and documents

Solvent-free, uncatalyzed asymmetric "ene" reactions of: N-Tert-butylsulfinyl-3,3,3-Trifluoroacetaldimines: A general approach to enantiomerically pure α-(trifluoromethyl)tryptamines

A novel approach to regioselectively substituted and stereoselectively α-Trifluoromethylated tryptamines is reported based on the ene reaction of Boc-protected 3-methyleneindolines with optically pure (R)-or (S)-Tert-butanesulfinyltrifluoroacetaldimine. B

Synthesis of new indole-based bisphosphonates and evaluation of their chelating ability in PE/CA-PJ15 cells

Bisphosphonates are the most important class of antiresorptive agents used against osteoclast-mediated bone loss, and, more recently, in oncology. These compounds have high affinity for calcium ions (Ca2+) and therefore target bone mineral, whe

New route to the 5,12-dihydro-7H-benzo[2,3]azepino[4,5-b]indol-6-one core via a tin-mediated indole synthesis

A new route to the paullone scaffold was designed. The key step consisted in a free radical indole formation from an o-alkenyl arylisonitrile followed by Stille coupling with N-Boc-o-iodoaniline. After deprotection and closure of the seven-membered ring by lactamisation, parent or cyano-substituted paullones were obtained in moderate to good yields. Georg Thieme Verlag Stuttgart.