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AB43312

497-06-3 | 3-Butene-1,2-diol

Packsize Purity Availability Price Discounted Price    Quantity
5g 97% in stock $13.00 $9.00 -   +
25g 97% in stock $29.00 $20.00 -   +
100g 97% in stock $86.00 $60.00 -   +
500g 97% in stock $309.00 $216.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB43312
Chemical Name: 3-Butene-1,2-diol
CAS Number: 497-06-3
Molecular Formula: C4H8O2
Molecular Weight: 88.1051
MDL Number: MFCD00239410
SMILES: OC(C=C)CO

 

Computed Properties
Complexity: 42.8  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 6  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 1  
XLogP3: -0.5  

 

 

Upstream Synthesis Route
  • 3-Butene-1,2-diol, also known as but-3-ene-1,2-diol, is a versatile compound commonly used in chemical synthesis. With its unique structure and reactivity, 3-Butene-1,2-diol serves as a crucial building block in the production of various chemical compounds.One of the key applications of 3-Butene-1,2-diol in chemical synthesis is its use as a precursor in the synthesis of complex organic molecules. By utilizing the double bonds present in the molecule, chemists can easily functionalize the compound to introduce diverse functional groups and create a wide range of derivatives. This flexibility makes 3-Butene-1,2-diol an invaluable starting material in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.Additionally, 3-Butene-1,2-diol can undergo various chemical transformations such as oxidation, reduction, and esterification, providing pathways to access a variety of compounds with different properties and applications. Its ability to participate in diverse reactions makes it a valuable tool for organic chemists seeking to design and synthesize novel molecules with specific functions.In summary, 3-Butene-1,2-diol plays a crucial role in chemical synthesis by serving as a versatile and reactive building block for the creation of complex organic compounds. Its utility in generating diverse derivatives and its compatibility with a wide range of synthetic strategies make it an essential component in the toolbox of synthetic chemists.
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