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AB75155

553-54-8 | Lithium benzoate

Packsize Purity Availability Price Discounted Price    Quantity
5g 99% in stock $8.00 $6.00 -   +
25g 99% in stock $16.00 $11.00 -   +
100g 99% in stock $62.00 $44.00 -   +
500g 99% in stock $157.00 $110.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB75155
Chemical Name: Lithium benzoate
CAS Number: 553-54-8
Molecular Formula: C7H5LiO2
Molecular Weight: 128.0544
MDL Number: MFCD00035540
SMILES: [O-]C(=O)c1ccccc1.[Li+]

 

Upstream Synthesis Route
  • Lithium benzoate is a versatile compound that finds widespread application in various chemical synthesis processes. As a key reagent in organic chemistry, it serves as a vital precursor in the production of numerous aromatic compounds and pharmaceuticals. Its unique properties make it a valuable addition to the toolbox of synthetic chemists.In chemical synthesis, lithium benzoate plays a crucial role as a source of both the benzoate anion and lithium cations. These components enable various reactions that lead to the creation of new C-C and C-O bonds. One common application is in the formation of aryl lithium compounds through metal-halogen exchange reactions. These aryl lithium species can then be employed in diverse transformations such as nucleophilic substitutions, additions to carbonyl compounds, and cross-coupling reactions.Additionally, lithium benzoate can be utilized in the preparation of carboxylic acid derivatives, including esters and amides. Through reactions with acyl chlorides or acid anhydrides, it serves as a valuable building block in the synthesis of a wide range of organic molecules. Furthermore, its role as a mild Lewis acid catalyst in certain transformations adds to its utility in promoting selective and efficient reactions.Overall, the application of lithium benzoate in chemical synthesis showcases its significance in enabling the creation of structurally diverse and functionally important molecules. Its versatility and reactivity make it a valuable tool for synthetic chemists seeking to develop innovative and efficient synthetic routes.
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