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1-(Trimethylsilyl)-1-propyne

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1-(Trimethylsilyl)-1-propyne Basic information

Product Name:
1-(Trimethylsilyl)-1-propyne
Synonyms:
  • Silane, trimethyl-1-propynyl-
  • 1-(trimethylsilyl)prop-1-yne
  • 1-(TRIMETYHLSILYL)PROPYNE
  • 1-(Trimethylsilyl)propyne,97%
  • trimethyl(prop-1-ynyl)silane
  • 1-Methyl-2- triMethylsilylacety
  • 1-(TRIMETHYLSILYL)-1-PROPYNE, 98%1-(TRIMETHYLSILYL)-1-PROPYNE, 98%1-(TRIMETHYLSILYL)-1-PROPYNE, 98%
  • (1-Propynyl)trimethylsilane
CAS:
6224-91-5
MF:
C6H12Si
MW:
112.25
EINECS:
228-314-5
Product Categories:
  • Si-(C)4 Compounds
  • Silicon Compounds (for Synthesis)
  • Acetylenes
  • Diyne Compounds (LB Films)
  • Ethynylsilanes
  • Synthetic Organic Chemistry
  • Functional Materials
  • Functionalized Acetylenes
  • LB Films
  • Si (Classes of Silicon Compounds)
Mol File:
6224-91-5.mol
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1-(Trimethylsilyl)-1-propyne Chemical Properties

Melting point:
-69°C
Boiling point:
99-100 °C (lit.)
Density 
0.758 g/mL at 25 °C (lit.)
vapor density 
>1 (vs air)
refractive index 
n20/D 1.417(lit.)
Flash point:
25 °F
storage temp. 
2-8°C
solubility 
Miscible with toluene.
form 
Liquid
Specific Gravity
0.758
color 
Clear colorless
Hydrolytic Sensitivity
4: no reaction with water under neutral conditions
BRN 
1071311
InChIKey
DCGLONGLPGISNX-UHFFFAOYSA-N
CAS DataBase Reference
6224-91-5(CAS DataBase Reference)
NIST Chemistry Reference
1-(Trimethylsilyl)-1-propyne(6224-91-5)
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Safety Information

Hazard Codes 
F,Xi
Risk Statements 
11-36/37/38
Safety Statements 
16-26-36-37/39
RIDADR 
UN 1993 3/PG 2
WGK Germany 
3
TSCA 
Yes
HazardClass 
3
PackingGroup 
II
HS Code 
29319090

MSDS

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1-(Trimethylsilyl)-1-propyne Usage And Synthesis

Chemical Properties

1-(Trimethylsilyl)-1-propyne is CLEAR COLOURLESS LIQUID

Uses

1-(Trimethylsilyl)propyne is used in the synthesis of alkynyl silane derivative.

Uses

1-Trimethylsilyl-1-propyne is employed in the preparation of alkynyl silane derivatives. It is also used to prepare highly substituted indenes using palladium-catalyzed carboannulation. Further, it plays an important role in the preparation of indenones through a rhodium-catalyzed reaction with 2-bromophenylboronic acids.

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