287172-66-1

Basic information

• Product Name: 1,2-BIS[2'-(TRIFLUOROMETHYL)PHENYL]ETHANE
• Synonyms: 1.2-BIS(2-TRIFLUOROMETHYLPHENYL)ETHAN;1,2-BIS-(2-TRIFLUOROMETHYLPHENYL)ETHANE;1,2-BIS[2'-(TRIFLUOROMETHYL)PHENYL]ETHANE;[2,2'-BIS(TRIFLUOROMETHYL)DIBENZYL];1,2-Bis[2'-(trifluoromethyl)phenyl]ethane97%;1,1'-Ethane-1,2-diylbis[2-(trifluoromethyl)benzene] 97%;1,1'-Ethane-1,2-diylbis[2-(trifluoromethyl)benzene]97%
• CAS NO: 287172-66-1
• Molecular Formula: C16H12F6
• Molecular Weight: 318.26
• Mol File: 287172-66-1.mol
• Article Data: 3

Chemical Properties

• Melting Point: 74-75°C
• Boiling Point: 270.7°Cat760mmHg
• Flash Point: 92.1°C
• Appearance: /
• Density: 1.273g/cm³
• Vapor Pressure: 0.0112mmHg at 25°C
• Refractive Index: 1.473
• CAS DataBase Reference: 1,2-BIS[2'-(TRIFLUOROMETHYL)PHENYL]ETHANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-BIS[2'-(TRIFLUOROMETHYL)PHENYL]ETHANE(287172-66-1)
• EPA Substance Registry System: 1,2-BIS[2'-(TRIFLUOROMETHYL)PHENYL]ETHANE(287172-66-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• HazardClass: IRRITANT
• Hazardous Substances Data: 287172-66-1(Hazardous Substances Data)

Usage

General Description

1,2-Bis[2'-(trifluoromethyl)phenyl]ethane is a chemical compound typically involved in scientific research and study. The term describes its molecular structure: each molecule has an ethane core, which is attached to two phenyl groups substituted with trifluoromethyl groups. Trifluoromethyl groups are very electron-withdrawing, which can impact the chemical's reactivity and other properties. However, detailed and specific information about this compound, including its uses, toxicity, and reactivity is not widely available in the public domain and likely requires professional scientific resources.

InChI:InChI=1/C16H12F6/c17-15(18,19)13-7-3-1-5-11(13)9-10-12-6-2-4-8-14(12)16(20,21)22/h1-8H,9-10H2

Upstream product

• 41949-98-8 methyl 1-bromocyclohexanecarboxylate 
• 395-44-8 o-trifluoromethylbenzyl bromide 
• 4294-57-9 para-methylphenylmagnesium bromide 

Relevant articles and documents

Formation of quaternary carbons through cobalt-catalyzed C(sp3)-C(sp3) Negishi cross-coupling

Formation of all-carbon-substituted quaternary carbons is a key challenge in organic and medicinal chemistry. We report a cobalt-catalyzed C(sp3)-C(sp3) cross-coupling that allows for the introduction of benzyl, heteroarylmethylzinc and allyl groups to halo-carbonyl substrates. The cross-coupling reaction is selective for C(sp3)-over C(sp2)-halides, in contrast to most used catalytic metals, and allows access to novel scaffolds of pharmaceutical interest. NMR mechanistic studies suggest the presence of Co(0) complexes as catalytic species. This journal is

IRON BISPHENOLATE COMPLEXES AND METHODS OF USE AND SYNTHESIS THEREOF

The present application, relates to iron bisphenolate complexes and methods of use and synthesis thereof. The iron complexes are prepared from tridentate or tetradentate ligands of Formula I: wherein R1 and R2 are as defined herein. Also provided are methods and processes of using the iron bisphenolate complexes as catalysts in cross-coupling reactions and in controlled radical polymerizations.