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76727-28-1

2H-1-Benzopyran-3-methanol,3,4-dihydro-

Catalog#: AR005J7T  |   CAS#: 76727-28-1  |   MDL#: MFCD04972641  |   MF: C10H12O2  |   MW: 164.2011

Packsize Purity Price Availability Quantity
50mg 95% $52.00 2-3 weeks Buy Now Add To Cart
100mg 95% $58.00 2-3 weeks Buy Now Add To Cart
250mg 95% $72.00 2-3 weeks Buy Now Add To Cart
500mg 95% $100.00 2-3 weeks Buy Now Add To Cart
1g 95% $119.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR005J7T
Chemical Name 2H-1-Benzopyran-3-methanol,3,4-dihydro-
CAS Number 76727-28-1
Molecular Formula C10H12O2
Molecular Weight 164.2011
MDL Number MFCD04972641
SMILES OCC1COc2c(C1)cccc2

2H-1-Benzopyran-3-methanol, 3,4-dihydro- is a versatile compound commonly used in chemical synthesis, particularly in the pharmaceutical and agrochemical industries. Due to its unique structure, this compound serves as a valuable building block for the synthesis of various biologically active molecules.In organic synthesis, 2H-1-Benzopyran-3-methanol, 3,4-dihydro- can be utilized as a key intermediate in the preparation of a wide range of heterocyclic compounds, such as pyrroles, pyridines, and indoles. Its functional groups and reactivity make it an excellent precursor for the introduction of additional substituents and functional groups, allowing for the creation of structurally diverse compounds with potential pharmacological or agricultural applications.Moreover, this compound can participate in different types of chemical reactions, including oxidation, reduction, and cyclization reactions, leading to the formation of complex molecular structures. Its incorporation in multistep synthesis pathways enables the efficient construction of target molecules with specific biological activities or agricultural properties.Overall, 2H-1-Benzopyran-3-methanol, 3,4-dihydro- plays a crucial role in the field of chemical synthesis by serving as a fundamental scaffold for the development of novel compounds with potential therapeutic or agricultural benefits. Its strategic positioning in synthetic routes highlights its importance as a valuable tool for the creation of diverse chemical entities with targeted functionalities.
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