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11,1,1-Trifluoroethane

  • CAS:420-46-2
  • purity:99%
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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

2-chloro-1,1,1-trifluoropropene
2730-62-3

2-chloro-1,1,1-trifluoropropene

1,3,3,3-tetrafluoro-propene
1645-83-6

1,3,3,3-tetrafluoro-propene

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

1,1,1,3,3,3-hexafluoropropane
690-39-1

1,1,1,3,3,3-hexafluoropropane

2,3,3,3-tetrafluoro-propene
754-12-1

2,3,3,3-tetrafluoro-propene

1,1,1,2,2-pentafluoropropane
1814-88-6

1,1,1,2,2-pentafluoropropane

Conditions
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.
2-chloro-1,1,1-trifluoropropene
2730-62-3

2-chloro-1,1,1-trifluoropropene

1,3,3,3-tetrafluoro-propene
1645-83-6

1,3,3,3-tetrafluoro-propene

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

2-chloro-1,1,1,2-tetrafluoropropane
421-73-8

2-chloro-1,1,1,2-tetrafluoropropane

1,1,1,3,3,3-hexafluoropropane
690-39-1

1,1,1,3,3,3-hexafluoropropane

2,3,3,3-tetrafluoro-propene
754-12-1

2,3,3,3-tetrafluoro-propene

1,1,1,2,2-pentafluoropropane
1814-88-6

1,1,1,2,2-pentafluoropropane

Conditions
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
    75-37-6

    1,1-difluoroethane

  • 75-68-3
    75-68-3

    1-Chloro-1,1-difluoroethane

  • 71-55-6
    71-55-6

    1,1,1-trichloroethane

  • 75-88-7
    75-88-7

    1,1,1-trifluoro-2-chloroethane

420-46-2 Downstream products

  • 421-06-7
    421-06-7

    2-bromo-1,1,1-trifluoroethane

  • 75-88-7
    75-88-7

    1,1,1-trifluoro-2-chloroethane

  • 75-38-7
    75-38-7

    Vinylidene fluoride

  • 374-12-9
    374-12-9

    1,1,2,2-tetrafluorocyclobutane

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