530080-19-4

Basic information

• Product Name: (4-BROMOPHENYL)(2,2,2-TRIFLUOROETHYL)SULFANE
• Synonyms: (4-BROMOPHENYL)(2,2,2-TRIFLUOROETHYL)SULFANE;1-Bromo-4-(2,2,2-trifluoroethylsulfanyl)benzene
• CAS NO: 530080-19-4
• Molecular Formula: C₈H₆BrF₃S
• Molecular Weight: 271.11
• Mol File: 530080-19-4.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (4-BROMOPHENYL)(2,2,2-TRIFLUOROETHYL)SULFANE(CAS DataBase Reference)
• NIST Chemistry Reference: (4-BROMOPHENYL)(2,2,2-TRIFLUOROETHYL)SULFANE(530080-19-4)
• EPA Substance Registry System: (4-BROMOPHENYL)(2,2,2-TRIFLUOROETHYL)SULFANE(530080-19-4)

Safety Data

• Hazardous Substances Data: 530080-19-4(Hazardous Substances Data)

Upstream product

• 433-06-7 2,2,2-Trifluoroethyl p-toluenesulfonate 
• 106-53-6 para-bromobenzenethiol 
• 421-06-7 2-bromo-1,1,1-trifluoroethane 
• 371-67-5 2,2,2-trifluorodiazoethane 
• 6334-55-0 allyl (4-bromophenyl)sulfide 
• 373-88-6 2,2,2-trifluroethylamine hydrochloride 

Downstream Products

• 648905-23-1 1-bromo-4-(2,2,2-trifluoro-ethanesulfonyl)-benzene 

Relevant articles and documents

Hemin Catalyzed Dealkylative Intercepted [2, 3]-Sigmatropic Rearrangement Reactions of Sulfonium Ylides with 2, 2, 2-Trifluorodiazoethane

A dealkylative intercepted [2, 3]-sigmatropic rearrangement reaction of allylic sulfides with 2, 2, 2-trifluorodiazoethane (CF3CHN2) is reported, the commercially available and biocompatible catalyst hemin was found to efficiently catalyze this transformation across a diverse set of allylic sulfides with in situ generated CF3CHN2, providing excellent yields (up to 99%) under mild condition without inert gas protection. In addition, CF3CHN2 exhibited unique reactivity toward this process compared with other frequently used diazo reagents. This work expands the range of carbene-mediated transformations catalyzed by hemin and introduces a concise and general strategy for exploiting new possibility of reactions concerning organosulfides. (Figure presented.).

Copper-Catalyzed Insertion into Heteroatom-Hydrogen Bonds with Trifluorodiazoalkanes

Copper-catalyzed Si-H, B-H, P-H, S-H, and N-H insertion reactions of 2,2,2-trifluoro-1-diazoethane and 1-aryl 2,2,2-trifluorodiazoethanes generated a large number of new fluorine-containing chemical entities for medicinal chemists. With selected Si-H and

OXAZOLIDINONE HYDROXAMIC ACID COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS

This invention pertains generally to treating bacterial infections using organic compounds of Formula I. In certain aspects, the invention pertains to treating infections caused by Gram-negative bacteria. (I) wherein X, Y, R1, R2, R3, R4 and R5 and defined herein.

SELECTIVE ESTROGEN RECEPTOR MODULATORS CONTAINING A PHENYLSULFONYL GROUP

The present invention relates to a selective estrogen receptor modulator of formula I or a pharmaceutical acid addition salt thereof; useful, e.g., for treating endometriosis and/or uterine leiomyoma/leiomyomata.