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(2-MERCAPTOETHYL)TRIMETHYLSILANE

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(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
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(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
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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
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

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(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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