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70505-77-0

3,4-dihydrospiro[chromene-2,1'-cyclopentan]-4-amine

Catalog#: AR00J8TM  |   CAS#: 70505-77-0  |   MDL#: MFCD10006200  |   MF: C13H17NO  |   MW: 203.2802

Packsize Purity Price Availability Quantity
50mg 93% $52.00 2-3 weeks Buy Now Add To Cart
100mg 93% $54.00 2-3 weeks Buy Now Add To Cart
250mg 93% $67.00 2-3 weeks Buy Now Add To Cart
500mg 93% $91.00 2-3 weeks Buy Now Add To Cart
1g 93% $111.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00J8TM
Chemical Name 3,4-dihydrospiro[chromene-2,1'-cyclopentan]-4-amine
CAS Number 70505-77-0
Molecular Formula C13H17NO
Molecular Weight 203.2802
MDL Number MFCD10006200
SMILES NC1CC2(CCCC2)Oc2c1cccc2

The compound 3,4-Dihydrospiro[1-benzopyran-2,1'-cyclopentane]-4-amine, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure containing both a spiro ring system and an amine functional group offers a wide range of opportunities for synthetic chemists.One key application of $name$ in chemical synthesis is its use as a starting material for the synthesis of complex heterocyclic compounds. By utilizing the amine group for various functional group transformations and the spiro ring system for stereochemical control, chemists can access a diverse array of structurally intricate molecules.Furthermore, the presence of the spiro[1-benzopyran-2,1'-cyclopentane] scaffold in $name$ imparts specific reactivity patterns that enable the construction of biologically active molecules, pharmaceutical intermediates, and natural product derivatives. Its presence in the molecular framework can influence the compound's physicochemical properties, such as lipophilicity and molecular recognition, making it a valuable component in drug discovery and development.In summary, the application of 3,4-Dihydrospiro[1-benzopyran-2,1'-cyclopentane]-4-amine in chemical synthesis extends beyond its individual structure, offering chemists a versatile platform for accessing diverse chemical space and creating novel compounds with potential biological activities.
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