1,1′-Oxybis[2,2,2-trifluoroethane]
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1,1′-Oxybis[2,2,2-trifluoroethane]
structure -
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CAS No:
333-36-8
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Formula:
C4H4F6O
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Chemical Name:
1,1′-Oxybis[2,2,2-trifluoroethane]
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Synonyms:
Ethane,1,1′-oxybis[2,2,2-trifluoro-;Ether,bis(2,2,2-trifluoroethyl);1,1′-Oxybis[2,2,2-trifluoroethane];SKF 6539;Bis(2,2,2-trifluoroethyl) ether;Fluorothyl;Fluroethyl;Flurothyl;Indoklon;2-(2,2,2-Trifluoroethoxy)-1,1,1-trifluoroethane;Hexafluorodiethyl ether;Flurotyl;HFE 356mff2;Idoklon;Indiklon;1,1,1-Trifluoro-2-(2,2,2-trifluoroethoxy)ethane
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CAS No:
Description
Fluorothyl (Flurothyl) is a inhaling volatile liquid.
Flurotyl is an ether.|Flurothyl is a convulsant primarily used in experimental animals. It was formerly used to induce convulsions as a alternative to electroshock therapy.|A convulsant primarily used in experimental animals. It was formerly used to induce convulsions as a alternative to electroshock therapy.
1,1′-Oxybis[2,2,2-trifluoroethane] Basic Attributes
182.06
182.06
9Z467FG2YK
760127
DTXSID5046516
2909199090
Characteristics
9.2
2.12760
clear colorless liquid
1.4171 g/cm3 @ Temp: 20 °C
<25 °C
63.9 °C
35 °F
n20/D 1.300(lit.)
Flammables area
155.99 mmHg
Abdominal-rat LD50: 1260 mg/kg; intravenous-mouse LD50: 46 mg/kg
Combustible in case of fire; burning produces toxic fluoride fumes
1.63e-13 cm3/molecule*sec
Safety Information
II
3.1
UN 3271 3/PG 2
3
11-36/37/38
16-26-36
KN3675000
F,Xi,T
Treasury is ventilated at low temperature and dry; stored separately from oxidants and food additives
Flammable/Toxic/Convulsant
P210-P261-P305 + P351 + P338
H225-H315-H319-H335
|Danger|H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]|P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P403+P235, P405, and P501|Aggregated GHS information provided by 41 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Substances that act in the brain stem or spinal cord to produce tonic or clonic convulsions, often by removing normal inhibitory tone. They were formerly used to stimulate respiration or as antidotes to barbiturate overdose. They are now most commonly used as experimental tools. (See all compounds classified as Convulsants.)
Fluorothyl
Computed Properties
Molecular Weight:182.06
XLogP3:2.3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:2
Exact Mass:182.01663372
Monoisotopic Mass:182.01663372
Topological Polar Surface Area:9.2
Heavy Atom Count:11
Complexity:98.7
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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1,1′-Oxybis[2,2,2-trifluoroethane]
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