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6144-93-0

4,4-Dimethyl-2-pentanol

Catalog#: AR003L4T  |   CAS#: 6144-93-0  |   MDL#: MFCD00004548  |   MF: C7H16O  |   MW: 116.2013

Packsize Purity Price Availability Quantity
250mg 98% $49.00 Global Stock Buy Now Add To Cart
1g 98% $130.00 Global Stock Buy Now Add To Cart
5g 98% $501.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003L4T
Chemical Name 4,4-Dimethyl-2-pentanol
CAS Number 6144-93-0
Molecular Formula C7H16O
Molecular Weight 116.2013
MDL Number MFCD00004548
SMILES CC(CC(C)(C)C)O

4,4-Dimethyl-2-pentanol, also known as Pivalol, is a versatile compound widely used in chemical synthesis processes. Due to its unique structure, this compound serves as an excellent solvent and reagent in various organic reactions. In particular, 4,4-Dimethyl-2-pentanol is commonly employed as a protecting group for alcohols in organic synthesis.In the field of organic chemistry, protecting groups play a crucial role in multi-step synthesis by temporarily masking reactive functional groups to prevent unwanted reactions. 4,4-Dimethyl-2-pentanol, with its bulky structure, can be easily attached to alcohol functional groups, forming stable acetals that shield the alcohol from undesired chemical transformations. This protection strategy allows chemists to selectively manipulate other parts of the molecule without affecting the alcohol group, enabling the synthesis of complex molecules with precision.Furthermore, 4,4-Dimethyl-2-pentanol exhibits low toxicity and high stability, making it a preferred choice for various chemical reactions requiring mild reaction conditions. Its compatibility with a wide range of functional groups and its ease of removal under mild acidic conditions make it a valuable asset in organic synthesis laboratories. From the synthesis of pharmaceuticals to the preparation of advanced materials, the application of 4,4-Dimethyl-2-pentanol in chemical synthesis underscores its significance in modern organic chemistry practices.
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GHS Pictogram N/A
UN# -
Hazard Statements -
Class -
Packing Group -

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