
Catalog Number	AR01ITIK
Chemical Name	2,3-dihydro-1H-inden-4-ylmethanol
CAS Number	65898-33-1
Molecular Formula	C10H12O
Molecular Weight	148.2017
MDL Number	MFCD22536334
SMILES	OCc1cccc2c1CCC2

The key applications of 2,3-dihydro-1H-inden-4-ylmethanol in chemical synthesis lie in its versatile reactivity and unique structural features. This compound serves as a valuable building block for the preparation of various organic molecules due to its ability to undergo different types of chemical transformations.One significant application of 2,3-dihydro-1H-inden-4-ylmethanol is its utilization in the synthesis of complex natural products and pharmaceutical intermediates. Its scaffold can be selectively functionalized to introduce specific functional groups or stereochemistry required for target molecule synthesis. Additionally, the indene moiety in this compound can participate in diverse chemical reactions, such as cycloadditions, oxidations, and reductions, expanding its synthetic utility.Moreover, 2,3-dihydro-1H-inden-4-ylmethanol can act as a chiral auxiliary in asymmetric synthesis. By exploiting its chirality, this compound enables the enantioselective synthesis of organic compounds, providing stereochemical control during key bond-forming steps. Its use as a chiral building block contributes to the development of advanced synthetic methodologies and the production of enantiopure compounds with high optical purity.Furthermore, 2,3-dihydro-1H-inden-4-ylmethanol finds application in the construction of functionalized heterocycles and complex molecules with biological activity. Its structural motif allows for the efficient diversification of chemical structures through strategic manipulation of its chemical reactivity, enabling the rapid and efficient synthesis of molecular libraries for drug discovery and material science research.

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Packsize	Purity	Price	Availability
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