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

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

• 111670-38-3 triphenyl-(6,6,6-trifluoro-hexyl)-phosphonium bromide 
• 111670-41-8 (Z)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-10,10,10-trifluoro-dec-4-enal 
• 111670-40-7 (Z)-(2S,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-11,11,11-trifluoro-undec-5-ene-1,2-diol 
• 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 
• 111670-42-9 [(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 
• 110-54-3 hexane 
• 1384267-42-8 C₁₈H₂₇F₃N₂O 
• 1441057-96-0 4-(6,6,6-trifluoro-hexyloxy)benzaldehyde 
• 1292808-51-5 C₃₆H₄₇F₃O₃Si 
• 1292808-50-4 C₃₇H₄₉F₃O₃Si 

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.

Angiotensin II antagonists

This invention provides novel phenyl and heterocyclic derivatives, their pharmaceutical formulations and their methods of use for antagonizing angiotensin II receptors in mammals.