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5445-45-4

(2,3-Dihydro-1H-inden-2-yl)methanol

Catalog#: AR00DBYY  |   CAS#: 5445-45-4  |   MDL#: MFCD08235017  |   MF: C10H12O  |   MW: 148.20168000000004

Packsize Purity Price Availability Quantity
100mg 98% $54.00 Global Stock Buy Now Add To Cart
250mg 98% $90.00 Global Stock Buy Now Add To Cart
1g 98% $277.00 Global Stock Buy Now Add To Cart
5g 98% $811.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DBYY
Chemical Name (2,3-Dihydro-1H-inden-2-yl)methanol
CAS Number 5445-45-4
Molecular Formula C10H12O
Molecular Weight 148.20168000000004
MDL Number MFCD08235017
SMILES OCC1Cc2c(C1)cccc2
NSC Number 22042

The application of (2,3-Dihydro-1H-inden-2-yl)methanol in chemical synthesis is highly versatile and valuable in various reactions. This compound, with its unique structure, serves as a key building block in the construction of complex organic molecules. Its presence can facilitate the formation of new carbon-carbon bonds, enabling the synthesis of intricate structures that would be challenging to access through other means.In organic chemistry, (2,3-Dihydro-1H-inden-2-yl)methanol can act as a versatile nucleophile or electrophile, participating in reactions such as nucleophilic addition, substitution, and elimination. Its reactivity allows for the introduction of functional groups at specific locations within a molecule, leading to the production of tailored compounds with desired properties.Furthermore, (2,3-Dihydro-1H-inden-2-yl)methanol can serve as a chiral auxiliary, imparting stereochemical control in asymmetric synthesis. By incorporating this compound into a reaction, chemists can influence the stereochemistry of the final product, enhancing the selectivity and efficiency of the synthesis process.Overall, the strategic use of (2,3-Dihydro-1H-inden-2-yl)methanol in chemical synthesis enables the elaboration of complex molecular architectures and the creation of diverse chemical entities with specific functionalities. Its versatile reactivity and role as a chiral building block make it a valuable tool for synthetic chemists seeking to access structurally intricate and biologically relevant compounds.
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GHS Pictogram N/A
UN# -
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Class -
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