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Cost-effective and customizable 11,1,1-Trifluoroethane 420-46-2 in stock
- Molecular Formula: C2H3F3
- Molecular Weight: 84.041
- Appearance/Colour: colourless gas
- Melting Point: -111 °C
- Boiling Point: -47 °C
- PSA: 0.00000
- Density: 1.078 g/cm3
- LogP: 1.56860
11,1,1-Trifluoroethane(Cas 420-46-2) Usage
|
General Description |
11,1,1-Trifluoroethane, also known as HFC-143a, is a fluorinated gas commonly used as a refrigerant in air conditioning and refrigeration systems. It is a colorless, odorless gas that is non-flammable and has a low toxicity. HFC-143a has a relatively low global warming potential, making it a popular alternative to ozone-depleting refrigerants such as chlorofluorocarbons (CFCs) and hydrochlorofluorocarbons (HCFCs). However, it still contributes to climate change as a greenhouse gas. Its use is regulated under the Montreal Protocol and its production is being phased out in many countries as part of efforts to reduce greenhouse gas emissions and mitigate climate change. |
InChI:InChI=1/C2H3F3/c1-2(3,4)5/h1H3
420-46-2 Relevant articles
Formation of CF3O- in the gas phase
Morris, Robert A.
, p. 8436 - 8442 (1999)
We report experimental studies of the fo...
Direct Superacid-Promoted Difluoroethylation of Aromatics
Artault, Maxime,Martin-Mingot, Agnès,Thibaudeau, Sébastien,Vitse, Kassandra
supporting information, (2021/12/22)
Under superacid conditions, aromatic ami...
Using Chlorotrifluoroethane for Trifluoroethylation of (Hetero)aryl Bromides and Chlorides via Nickel Catalysis
Li, Xuefei,Gao, Xing,He, Chun-Yang,Zhang, Xingang
supporting information, p. 1400 - 1405 (2021/02/20)
A nickel-catalyzed reductive cross-coupl...
C(sp3)-CF3Reductive Elimination from a Five-Coordinate Neutral Copper(III) Complex
Liu, Shuanshuan,Liu, Shuanshuan,Liu, He,Liu, Shihan,Lu, Zehai,Lu, Changhui,Leng, Xuebing,Lan, Yu,Shen, Qilong
supporting information, p. 9785 - 9791 (2020/07/10)
The reductive elimination from a high-va...
Improved Access to Organo-Soluble Di- and Tetrafluoridochlorate(I)/(III) Salts
Kaupp, M.,Müller, R.,Pr?hm, P.,Riedel, S.,Schattenberg, C. J.,Schmid, J. R.,Sonnenberg, K.,Steinhauer, S.,Vo?nacker, P.
supporting information, p. 16002 - 16006 (2020/07/20)
A facile one-pot gram-scale synthesis of...
420-46-2 Process route
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-
2730-62-3
2-chloro-1,1,1-trifluoropropene
-
-
1645-83-6
1,3,3,3-tetrafluoro-propene
-
-
420-46-2
2,2,2-trifluoroethanol
-
-
690-39-1
1,1,1,3,3,3-hexafluoropropane
-
-
754-12-1
2,3,3,3-tetrafluoro-propene
-
-
1814-88-6
1,1,1,2,2-pentafluoropropane
| Conditions | Yield |
|---|---|
|
With
chromium(III) oxide; hydrogen fluoride; oxygen;
at 350 ℃;
for 0.0025h;
|
30 %Chromat.
8.8 %Chromat. 23 %Chromat. 7.2 %Chromat. 5.8 %Chromat. |
-
-
2730-62-3
2-chloro-1,1,1-trifluoropropene
-
-
1645-83-6
1,3,3,3-tetrafluoro-propene
-
-
420-46-2
2,2,2-trifluoroethanol
-
-
421-73-8
2-chloro-1,1,1,2-tetrafluoropropane
-
-
690-39-1
1,1,1,3,3,3-hexafluoropropane
-
-
754-12-1
2,3,3,3-tetrafluoro-propene
-
-
1814-88-6
1,1,1,2,2-pentafluoropropane
| Conditions | Yield |
|---|---|
|
With
chromium(III) oxide; hydrogen fluoride; oxygen;
at 350 ℃;
for 0.0025h;
Reagent/catalyst;
|
30 %Chromat.
8.6 mg 23 %Chromat. 6.4 %Chromat. 8.7 %Chromat. 8.7 %Chromat. |
420-46-2 Upstream products
-
75-37-6
1,1-difluoroethane
-
75-68-3
1-Chloro-1,1-difluoroethane
-
71-55-6
1,1,1-trichloroethane
-
75-88-7
1,1,1-trifluoro-2-chloroethane
420-46-2 Downstream products
-
421-06-7
2-bromo-1,1,1-trifluoroethane
-
75-88-7
1,1,1-trifluoro-2-chloroethane
-
75-38-7
Vinylidene fluoride
-
374-12-9
1,1,2,2-tetrafluorocyclobutane
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