335452
Lithium (trimethylsilyl)acetylide solution
0.5 M in THF
Synonym(s):
(Trimethylsilyl)ethynyllithium
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Recommended Products
form
liquid
Quality Level
concentration
0.5 M in THF
density
0.88 g/mL at 25 °C
SMILES string
[Li]C#C[Si](C)(C)C
InChI
1S/C5H9Si.Li/c1-5-6(2,3)4;/h2-4H3;
InChI key
ZVXXEONXFWSCIZ-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
Lithium (trimethylsilyl)acetylide can be used as a reagent:
- In the transmetalation and nucleophilic displacement reactions.
- To prepare propargylic alcohol derivatives by reacting with aldehydes and ketones.
- To synthesize α,βynones by treating with Weinreb amide or with isoxazolidide.
- Along with Grignard reagent to convert γ- and δ-thiolactams to thioiminium salts, which are employed as key intermediates to produce disubstituted pyrrolidines.
Reacts with halotriazines to produce conductive, anisotropic carbon-nitrogen materials.
Packaging
The 25 mL Sure/Seal™ bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.
Legal Information
Sure/Seal is a trademark of Sigma-Aldrich Co. LLC
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Supplementary Hazards
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
-9.4 °F - closed cup
Flash Point(C)
-23 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Chemistry of Materials, 6, 636-636 (1994)
Lithium (Trimethylsilyl) acetylide
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2001)
Sequential addition reaction of lithium acetylides and Grignard reagents to thioiminium salts from thiolactams leading to 2, 2-disubstituted cyclic amines
Tetrahedron, 62(26), 6312-6320 (2006)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service