(2-MERCAPTOETHYL)TRIMETHYLSILANE
(2-MERCAPTOETHYL)TRIMETHYLSILANE Basic information
- Product Name:
- (2-MERCAPTOETHYL)TRIMETHYLSILANE
- Synonyms:
-
- 2-(trimethylsilyl)-ethanethio
- BEST
- (2-MERCAPTOETHYL)TRIMETHYLSILANE
- (2-Mercaptoethyl)trimethylsilane(2-Trimethylsilylethanethiol)
- 2-(TRIMETHYLSILYL)ETHANETHIOL
- 2-TRIMETHYLSILANYL-ETHANETHIOL
- ETHYLTHIOTRIMETHYLSILANE 97%
- (2-Mercaptoethyl)trimethylsilane, BEST
- CAS:
- 18143-30-1
- MF:
- C5H14SSi
- MW:
- 134.32
- Mol File:
- 18143-30-1.mol
(2-MERCAPTOETHYL)TRIMETHYLSILANE Chemical Properties
- Boiling point:
- 144-146 °C(lit.)
- Density
- 0.839 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.454(lit.)
- Flash point:
- 85 °F
- storage temp.
- 2-8°C
- solubility
- Soluble in MeOH, CH2Cl2, THF, and most organic solvents.
- pka
- 10.80±0.10(Predicted)
- BRN
- 1732126
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 10-36/37/38
- Safety Statements
- 26-36
- RIDADR
- UN 1993 3/PG 3
- WGK Germany
- 3
- RTECS
- KJ2621000
- F
- 13
- HazardClass
- 3.2
- PackingGroup
- III
- Toxicity
- mouse,LD50,intraperitoneal,2500mg/kg (2500mg/kg),Doklady Akademii Nauk SSSR. Proceedings of the Academy of Sciences of the USSR. For English translation, see DBIOAM and DKBSAS. Vol. 229, Pg. 1011, 1976.
MSDS
- Language:English Provider:SigmaAldrich
(2-MERCAPTOETHYL)TRIMETHYLSILANE Usage And Synthesis
Physical properties
bp 144–146 °C [52–54 °C (25 Torr)]; d 0.850.
Uses
2-(Trimethylsilyl)ethanethiol is a reagent used as a monoprotected sulfide dianion equivalent for the two-step installation of a divalent sulfur atom into organic molecules. It participates in the reactions of Thiol Substitution Reactions, Source of Sulfur Acid Derivatives, etc.
Preparation
The high commercial cost of 2-(trimethylsilyl)ethanethiol necessitates methods for its lab scale synthesis. The radical addition of thiolacetic acid to vinyltrimethylsilane occurs thermally to afford a 9:1 ratio of regioisomers, the 1- and 2-(trimethylsilyl)ethyl thiolesters of acetic acid (eq 1). Photochemical initiation may improve the ratio of regioisomers obtained. Purification of the thiolacetate by careful fractional distillation should be performed prior to conversion to the thiol in order to ensure high purity. The conversion to thiol is best performed with LAH3 or methanolic K2CO3, but ammonolysis may also be suitable. Saponification with KOH in water/ethanol is slightly less efficient. Direct radical addition of liquid H2S to vinyl trimethylsilane has been demonstrated, but the procedure is low-yielding and inconvenient.
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