(Trimethylsilyl)acetylene
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(Trimethylsilyl)acetylene
structure -
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CAS No:
1066-54-2
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Formula:
C5H10Si
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Chemical Name:
(Trimethylsilyl)acetylene
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Synonyms:
Silane,ethynyltrimethyl-;Ethynyltrimethylsilane;Trimethylethynylsilane;(Trimethylsilyl)ethyne;1-(Trimethylsilyl)acetylene;1-Trimethylsilylethyne;(Trimethylsilyl)acetylene;Trimethylsilanylethyne;Acetylenyltrimethylsilane;(Trimethylsilanyl)acetylene;2,2-Dimethyl-2-sila-3-butyne;TMS-acetylene;959419-58-0;1042949-84-7;1277091-35-6
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CAS No:
Description
CLEAR COLORLESS LIQUIDTrimethylsilylacetylene is a silican-protected group, also known as trimethylethynylsilane, trimethylethynyl silicon and ethynyltrimethylsilane. It is a colorless transparent liquid at room temperature. It could be used to synthesize parazole by the addition of 1,3-bipolar ring of acetylene diazide. It is also the substrate of nickel catalyzed reaction and benzonitrile coupling reaction.
Characteristics
0
1.49700
colorless liquid
0.709 g/cm3
>0°C
52 °C
<−30 °F
n 20/D 1.388(lit.)
Solubility in water: reaction.;Miscible with organic solvents.
2-8°C
4.18 psi ( 20 °C)
Safety Information
II
3
UN 1993 3/PG 2
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11-36/37/38
16-26-36
F,Xi
Flammable/Irritant
Materials containing similar functional groups can decompose at elevated temperatures. Has not been fully evaluated.
P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P403+P235, P405, P501
H225
|Danger|H225 (70%): Highly Flammable liquid and vapor [Danger Flammable liquids]|P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P403+P235, P405, and P501|Aggregated GHS information provided by 80 companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
(Trimethylsilyl)acetylene Use and Manufacturing
Ethynyltrimethylsilane was used in:? microwave-assisted, one-pot, three-step Sonogashira cross-coupling-desilylation-cycloaddition reaction for the preparation of 1,4-disubstituted 1,2,3-triazoles synthesis of poly(ethynyltrimethylsilane) containing Pd (II) coordination sites pyrazole synthesis via 1,3-dipolar cycloaddition of diazo compounds to acetylenes
Silane, ethynyltrimethyl-: ACTIVE
Computed Properties
Molecular Weight:98.22
Rotatable Bond Count:1
Exact Mass:98.055176853
Monoisotopic Mass:98.055176853
Heavy Atom Count:6
Complexity:77.8
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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