Methyllithium, Promotion Season Now in Store and Free Sample for Testing with Factory Price
- Chemical Name: Methyllithium
- CAS No.:917-54-4
- Molecular Fomula:CH3Li
- Molecular weight:21.98
- Appearance:Colorless to yellow
- Sample: Available
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Description of Methyllithium
Lowhalide is the simplest organolithium reagent with the empirical formula CH3Li. This s-block organometallic compound adopts an oligomeric structure both in solution and in the solid state. This highly reactive compound, invariably used as a solution in ethers, is a reagent in organic synthesis as well as organometallic chemistry.
Basic Info of Methyllithium
Basic Info
Numbering system
Properties
Safety Info
Basic Info
Chemical Name | Lowhalide |
Synonyms | Lithium,methyl;MeLi;Lithium methanide;methyllitium;Methyl lithium;Expand |
CAS No. | 917-54-4 |
Molecular Formula | CH3Li |
Molecular Weight | 21.97550 |
PSA | 0.00000 |
LogP | 0.58380 |
Numbering system
EINECS number | 213-026-4 |
Properties
Appearance & Physical State | Colorless solid |
Density | 0.7 |
Boiling Point | 35ºC |
Melting Point | 70-71ºC |
Flash Point | -17ºC |
Storage Condition | 2-8ºC |
Vapor Density | 3 (vs air) |
Safety Info
Appearance & Physical State | Colorless solid |
Density | 0.7 |
Boiling Point | 35ºC |
Melting Point | 70-71ºC |
Flash Point | -17ºC |
Storage Condition | 2-8ºC |
Vapor Density | 3 (vs air) |
What is Methyllithium?
With the progress of science and technology and the development of society, chemical products have invariably permeated our daily lives, in medicine, food, cosmetics, electronics, industry, and other areas, becoming an essential part of our lives. One such product is it which has developed particularly rapidly in recent years. Do you know about it?
The official answer:Organometallic compounds belonging to the s-zone, either in solid or solution in the oligomeric state. It is often used in the synthesis of ethers and organic synthesis and organometallic chemistry.
What’s the application of Methyllithium?
Methyl lithium can methylate a wide range of functional groups, can remove protecting groups, synthesize other methylated organometallic reagents, can act as a base and reduce transition metals, etc. Solvents and halogens have a strong influence on the reactions using non-solvated Lowhalide.
Conclusion
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