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PROPARGYLTRIMETHYLSILANE

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PROPARGYLTRIMETHYLSILANE Basic information

Product Name:
PROPARGYLTRIMETHYLSILANE
Synonyms:
  • Propargyltrimethylsilane, stabilized, 80-90%
  • PropargyltriMethylsilane, stabilized, 8
  • triMethyl(prop-2-yn-1-yl)silane
  • TriMethyl(propargyl)silane contains 500 ppM BHT as stabilizer
  • Silane,trimethyl-2-propyn-1-yl-
  • 3-TRIMETHYLSILYL-1-PROPYNE
  • 3-(TRIMETHYLSILYL)PROPYNE
  • 2-PROPYNYL-TRIMETHYLSILANE
CAS:
13361-64-3
MF:
C6H12Si
MW:
112.25
EINECS:
236-427-6
Mol File:
13361-64-3.mol
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PROPARGYLTRIMETHYLSILANE Chemical Properties

Melting point:
148-151 °C(Solv: ethyl ether (60-29-7))
Boiling point:
91-93 °C (lit.)
Density 
0.753 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.413(lit.)
Flash point:
13 °F
storage temp. 
-20°C
solubility 
sol ether, THF, CH2Cl2.
form 
Liquid
color 
Clear yellow
BRN 
2036316
CAS DataBase Reference
13361-64-3
EPA Substance Registry System
Silane, trimethyl-2-propynyl- (13361-64-3)
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Safety Information

Hazard Codes 
F,Xi
Risk Statements 
11-36/37/38
Safety Statements 
16-26-36
RIDADR 
UN 1993 3/PG 2
WGK Germany 
3
HazardClass 
3.1
PackingGroup 
II
HS Code 
29310099

MSDS

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PROPARGYLTRIMETHYLSILANE Usage And Synthesis

Chemical Properties

Clear yellow liquid

Physical properties

bp 91–93 °C/760 mmHg; 40 °C/140 mmHg; d 0.753 g mL?1; nD 20 1.4140.

Uses

3-Trimethylsilyl-1-propyne is used as propargylation agent; allenylation agent; can give addition reactions on the triple bond. It takes part in the following reactions: Propargylation Reactions, Alkylation Reactions, Reactions with Epoxides,Reactions with Aldehydes and Ketones, Reactions with Chloroformates, Reactions with Polyoxymethylene and Amines, Allenylation Reactions, Substitution Reactions, Reactions with Acetals and Hemiacetals, Reactions with Aldehydes and Ketones, Reactions with in situ Generated Iminium and α-Acyl Iminium Ions, Reactions with Acid Chlorides, Reactions with Conjugated Heteroatomic Systems, Reactions of the Triple Bond etc.

Uses

Trimethyl(propargyl)silane is suitable for use in the synthesis of diverse end-functionalized (ω-carboxyl, ω-hydroxy, ω-methyl-vinyl, ω-trimethylsilane, and ω-glycidyl-ether) via ′′click′′ reaction. It may be used in the synthesis of γ-allenyl-GABA (γ-aminobutyric acid), via Lewis acid mediated reaction with ω-ethoxy lactams.

Preparation

The main method of preparation is shown in eq 1. The title reagent can be obtained by other methods, but in poor yields.

General Description

Trimethyl(propargyl)silane (2-Propynyl-trimethylsilane) is a clear colorless liquid and contains 500ppm of butylated hydroxytoluene (BHT) as stabilizer. It undergoes GaCl3-catalyzed dehydrogenation reaction with aldimines to afford 4-methylquinoline.

Purification Methods

Fractionally distil it and add 2,6-di-tert-butyl-p-cresol (~0.5%) to stabilise it. [Petrov et al. Doklady Acad Nauk USSR 93 293 1953, cf Chem Abstr 48 13616 1954, Beilstein 4 IV 3938.]

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