ChemicalBook--->CAS DataBase List--->1544-53-2

1544-53-2

1544-53-2 Structure

1544-53-2 Structure
IdentificationBack Directory
[Name]

2,2,2-TRIFLUOROETHANETHIOL
[CAS]

1544-53-2
[Synonyms]

2,2,2-Trifluoroethanthiol
2,2,2-TRIFLUOROETHANETHIOL
Ethanethiol, 2,2,2-trifluoro-
2,2,2-TRIFLUOROETHANETHIOL 95%
[Molecular Formula]

C2H3F3S
[MDL Number]

MFCD00134386
[MOL File]

1544-53-2.mol
[Molecular Weight]

116.11
Chemical PropertiesBack Directory
[Melting point ]

51.3-52.3 °C
[Boiling point ]

34-35 °C (lit.)
[density ]

1.305 g/mL at 25 °C (lit.)
[vapor pressure ]

7.85 psi ( 20 °C)
[refractive index ]

n20/D 1.352(lit.)
[Fp ]

−11 °F
[form ]

liquid
[pka]

7.60±0.10(Predicted)
[InChI]

1S/C2H3F3S/c3-2(4,5)1-6/h6H,1H2
[InChIKey]

RYRLLAOLJVDVNN-UHFFFAOYSA-N
[SMILES]

FC(F)(F)CS
Safety DataBack Directory
[Hazard Codes ]

F+,Xn
[Risk Statements ]

12-20/21/22-36/37/38
[Safety Statements ]

16-33-38
[RIDADR ]

UN 3336 3/PG 1
[WGK Germany ]

3
[HazardClass ]

3.1
[PackingGroup ]

I
[Storage Class]

3 - Flammable liquids
[Hazard Classifications]

Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Flam. Liq. 1
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]


  • Advancements in Peptide Synthesis: A novel synthesis of β-thiol phenylalanine showcases the use of 2,2,2-Trifluoroethanethiol in facilitating one-pot ligation-desulfurization chemistry. This technique is pivotal for developing new peptide-based pharmaceuticals, enhancing both the efficiency and versatility of peptide synthesis (Malins et al., 2015).

[General Description]

2,2,2-Trifluoroethanethiol is basic in nature and forms charge transfer complexes with molecular iodine.
Spectrum DetailBack Directory
[Spectrum Detail]

2,2,2-TRIFLUOROETHANETHIOL(1544-53-2)1HNMR
2,2,2-TRIFLUOROETHANETHIOL(1544-53-2)IR
2,2,2-TRIFLUOROETHANETHIOL(1544-53-2)Raman
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