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Home  > 1,1,3,3-Tetramethylguanidine

AB56851

80-70-6 | 1,1,3,3-Tetramethylguanidine

Packsize Purity Availability Price Discounted Price    Quantity
5g 97% in stock $12.00 $8.00 -   +
25g 97% in stock $32.00 $22.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB56851
Chemical Name: 1,1,3,3-Tetramethylguanidine
CAS Number: 80-70-6
Molecular Formula: C5H13N3
Molecular Weight: 115.1768
MDL Number: MFCD00075588
SMILES: CN(C(=N)N(C)C)C
NSC Number: 148309

 

Computed Properties
Complexity: 75.7  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 8  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 0.4  

 

 

Upstream Synthesis Route
  • 1,1,3,3-Tetramethylguanidine, also known as TMG, is a versatile organic compound commonly used in chemical synthesis as a strong, non-nucleophilic base. Its unique structure and properties make it a valuable reagent in various reactions, particularly in organic transformations where high basicity and steric hindrance are required.In organic synthesis, TMG is frequently employed as a base catalyst in reactions such as deprotonation, elimination, and condensation. Due to its strong basicity and lack of nucleophilicity, TMG is an ideal choice for promoting reactions that involve sensitive functional groups or require precise control over selectivity. Its bulky structure helps to prevent unwanted side reactions by hindering unwanted interactions with neighboring functional groups or substrates.Additionally, 1,1,3,3-Tetramethylguanidine is often used in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals where the precise manipulation of reaction conditions is crucial to achieving high yields and selectivity. Its application extends to various organic transformations including the formation of carbon-carbon bonds, the activation of electrophiles, and the deprotection of functional groups.Overall, TMG plays a significant role in modern organic synthesis by providing chemists with a powerful tool to facilitate complex reactions with enhanced control and efficiency.
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