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144282-37-1

Carbamic acid, N-[(7S)-5-(phenylmethyl)-5-azaspiro[2.4]hept-7-yl]-, 1,1-dimethylethyl ester

Catalog#: AR001JX9  |   CAS#: 144282-37-1  |   MDL#: MFCD17214772  |   MF: C18H26N2O2  |   MW: 302.4112

Packsize Purity Price Availability Quantity
100mg 95% $13.00 Global Stock Buy Now Add To Cart
250mg 95% $13.00 Global Stock Buy Now Add To Cart
1g 95% $38.00 Global Stock Buy Now Add To Cart
5g 95% $128.00 Global Stock Buy Now Add To Cart
10g 95% $252.00 Global Stock Buy Now Add To Cart
25g 95% $614.00 Global Stock Buy Now Add To Cart
50g 95% $1,207.00 Global Stock Buy Now Add To Cart
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Catalog Number AR001JX9
Chemical Name Carbamic acid, N-[(7S)-5-(phenylmethyl)-5-azaspiro[2.4]hept-7-yl]-, 1,1-dimethylethyl ester
CAS Number 144282-37-1
Molecular Formula C18H26N2O2
Molecular Weight 302.4112
MDL Number MFCD17214772
SMILES O=C(OC(C)(C)C)N[C@@H]1CN(CC21CC2)Cc1ccccc1

The (S)-tert-Butyl (5-benzyl-5-azaspiro[2.4]heptan-7-yl)carbamate is a versatile compound widely utilized in chemical synthesis. It serves as a valuable building block in the creation of complex organic molecules due to its unique structural characteristics and reactivity. In particular, this compound is often employed in the synthesis of pharmaceuticals, agrochemicals, and specialized materials.One of the key applications of (S)-tert-Butyl (5-benzyl-5-azaspiro[2.4]heptan-7-yl)carbamate lies in its role as a chiral auxiliary. By utilizing its stereochemical properties, chemists can control the stereochemistry of reactions, enabling the production of enantiomerically pure compounds. This is crucial in the pharmaceutical industry, where the biological activity of molecules is highly dependent on their stereochemistry.Furthermore, this compound can act as a protecting group for amines in organic synthesis. By temporarily masking the amino group with the (S)-tert-Butyl (5-benzyl-5-azaspiro[2.4]heptan-7-yl)carbamate moiety, chemists can selectively manipulate other functional groups without affecting the amine. Subsequent deprotection of the carbamate group allows for the controlled release of the amine, leading to the desired product.In summary, the (S)-tert-Butyl (5-benzyl-5-azaspiro[2.4]heptan-7-yl)carbamate plays a crucial role in chemical synthesis by serving as a chiral building block and a versatile amine protecting group. Its strategic use in various synthetic transformations highlights its importance in the creation of complex organic molecules with specific stereochemical and functional group requirements.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302
Precautionary Statements P280-P305+P351+P338
Class N/A
Packing Group N/A

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