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AD59662

1206968-77-5 | 2-(5-Bromopyridin-2-yl)ethanol

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $49.00 $34.00 -   +
250mg 95% in stock $75.00 $52.00 -   +
500mg 95% in stock $88.00 $62.00 -   +
1g 95% in stock $92.00 $64.00 -   +
5g 95% in stock $372.00 $260.00 -   +
25g 95% in stock $1,480.00 $1,036.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AD59662
Chemical Name: 2-(5-Bromopyridin-2-yl)ethanol
CAS Number: 1206968-77-5
Molecular Formula: C7H8BrNO
Molecular Weight: 202.0485
MDL Number: MFCD09999981
SMILES: OCCc1ccc(cn1)Br

 

Computed Properties
Complexity: 99.6  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 1.2  

 

 

Upstream Synthesis Route
  • 2-(5-Bromopyridin-2-yl)ethanol is a valuable chemical compound commonly used in chemical synthesis processes. This compound serves as a versatile building block in organic synthesis, with its unique structure enabling it to participate in a wide range of reactions and transformations.In chemical synthesis, 2-(5-Bromopyridin-2-yl)ethanol is often employed as a reagent for the preparation of various functionalized molecules. Its bromopyridine moiety can undergo substitution reactions, allowing for the introduction of different functional groups at the 2-position of the pyridine ring. This versatility makes it a valuable tool for the synthesis of complex organic molecules with specific structural features.Furthermore, the presence of the hydroxyl group in 2-(5-Bromopyridin-2-yl)ethanol adds an additional level of reactivity to the compound. The hydroxyl group can participate in various chemical transformations, such as esterification or oxidation reactions, further expanding the synthetic utility of this compound.Overall, 2-(5-Bromopyridin-2-yl)ethanol is a key component in the toolbox of synthetic chemists, offering a range of possibilities for the construction of diverse chemical structures in the laboratory setting. Its versatility, reactivity, and compatibility with various synthetic methodologies make it an indispensable compound for modern organic synthesis techniques.
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