5-[tert-butyl(dimethyl)silyl]oxy-2-oxo-3,3a,4,5,6,6a-hexahydrocyclopenta[b]furan-4-carbaldehyde


Chemical Name: 5-[tert-butyl(dimethyl)silyl]oxy-2-oxo-3,3a,4,5,6,6a-hexahydrocyclopenta[b]furan-4-carbaldehyde
CAS Number: 64091-14-1
Product Number: AG00EBKZ(AGN-PC-00KKEC)
Synonyms:
MDL No:
Molecular Formula: C14H24O4Si
Molecular Weight: 284.4235

Identification/Properties


Computed Properties
Molecular Weight:
284.427g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
284.144g/mol
Monoisotopic Mass:
284.144g/mol
Topological Polar Surface Area:
52.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
385
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
4
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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Chemical Structure



The compound (3aR,4R,5R,6aS)-5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]hexahydro-2-oxo-2H-cyclopenta[b]furan-4-carboxaldehyde, commonly referred to as $name$, is a versatile reagent utilized in chemical synthesis. This compound serves as a key building block in organic reactions due to its unique structural features and reactivity. In synthetic methodologies, $name$ acts as a valuable precursor for the introduction of functional groups, enabling the formation of complex molecular structures. Its strategic incorporation in various chemical transformations allows for the selective modification of target molecules, facilitating the synthesis of novel compounds with tailored properties. As a valuable tool in organic synthesis, $name$ plays a crucial role in the development of new molecules for pharmaceuticals, materials science, and other research areas. By leveraging the chemical reactivity of $name$, chemists can efficiently access a diverse array of molecular architectures, driving innovation and discovery in the field of chemistry.