111670-37-2

Basic information

• Product Name: 6-BROMO-1,1,1-TRIFLUOROHEXANE
• Synonyms: 6-BROMO-1,1,1-TRIFLUOROHEXANE
• CAS NO: 111670-37-2
• Molecular Formula: C₆H₁₀BrF₃
• Molecular Weight: 219.04
• Mol File: 111670-37-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 153.9±8.0 °C(Predicted)
• Appearance: /
• Density: 1.393±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 6-BROMO-1,1,1-TRIFLUOROHEXANE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-BROMO-1,1,1-TRIFLUOROHEXANE(111670-37-2)
• EPA Substance Registry System: 6-BROMO-1,1,1-TRIFLUOROHEXANE(111670-37-2)

Safety Data

• Hazardous Substances Data: 111670-37-2(Hazardous Substances Data)

Upstream product

• 4224-70-8 6-bromohexanoic acid 

Downstream Products

• 110-54-3 hexane 
• 1292808-50-4 C₃₇H₄₉F₃O₃Si 
• 1292808-51-5 C₃₆H₄₇F₃O₃Si 
• 1441057-96-0 4-(6,6,6-trifluoro-hexyloxy)benzaldehyde 
• 1384267-42-8 C₁₈H₂₇F₃N₂O 
• 111670-42-9 [(3Z,5E,7E,11Z)-(2R,9R)-2,9-Bis-(tert-butyl-diphenyl-silanyloxy)-17,17,17-trifluoro-heptadeca-3,5,7,11-tetraenylsulfanyl]-acetic acid methyl ester 
• 111670-42-9 [(3Z,5E,7E,11Z)-(2R,9R)-2,9-Bis-(tert-butyl-diphenyl-silanyloxy)-17,17,17-trifluoro-heptadeca-3,5,7,11-tetraenylsulfanyl]-acetic acid methyl ester 
• 111670-39-4 tert-Butyl-[(Z)-(R)-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-9,9,9-trifluoro-non-3-enyloxy]-diphenyl-silane 
• 111670-40-7 (Z)-(2S,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-11,11,11-trifluoro-undec-5-ene-1,2-diol 
• 111670-41-8 (Z)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-10,10,10-trifluoro-dec-4-enal 
• 111670-38-3 triphenyl-(6,6,6-trifluoro-hexyl)-phosphonium bromide 

Relevant articles and documents

Aromatic ketones and uses thereof

Aromatic ketones having an extended fluoro-alkyl or fluoro-alkoxy moiety are disclosed. In particular aspects, the compounds comprise substituted 9-acridone, 9-xanthone, 4(1H)-quinolone, 4(1H) pyridone, 1,4-naphthoquinone, 9,10-anthraquinone derivatives. These preparations possess potent pharmacological activity for inhibiting malaria and mosquito-borne (Plasmodium) diseases. The haloalkyl/alkoxy aromatic compounds possess significant pharmacological activity, with IC50 values in the nanomolar and sub-nanomolar range, and reduced toxicity against host derived cells and tissues. Methods of using the fluoro-alkyl/alkoxy aromatic compounds in the treatment of malaria and other human and animal diseases are also disclosed. Agricultural uses of the fluoro-alkyl/alkoxy aromatic compounds, such as in control of fungal diseases and in the production of important commercial crops (apples, etc.), are also presented.

Total synthesis of leukotriene B4 analogues: 3-thia-LTB4 and 3-thia-20,20,20-trifluoro-LTB4

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