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AA32927

1197239-37-4 | tert-Butyl (3-aminocyclopentyl)carbamate hydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $63.00 $45.00 -   +
250mg 97% in stock $84.00 $59.00 -   +
1g 97% in stock $223.00 $156.00 -   +
5g 97% in stock $788.00 $551.00 -   +
10g 97% in stock $1,409.00 $987.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA32927
Chemical Name: tert-Butyl (3-aminocyclopentyl)carbamate hydrochloride
CAS Number: 1197239-37-4
Molecular Formula: C10H21ClN2O2
Molecular Weight: 236.7389
MDL Number: MFCD09759162
SMILES: NC1CCC(C1)NC(=O)OC(C)(C)C.Cl

 

Upstream Synthesis Route
  • The tert-Butyl (3-aminocyclopentyl)carbamate hydrochloride serves as a versatile reagent in chemical synthesis due to its unique structural properties. This compound is commonly utilized in organic chemistry as a protecting group for amines, allowing for selective manipulation of amine functionalities within complex molecule synthesis. By forming a stable carbamate linkage, tert-Butyl (3-aminocyclopentyl)carbamate hydrochloride provides a temporary shield to the amine group, protecting it from unwanted reactions during various synthetic transformations. This protective group strategy enables chemists to control the reactivity of the amine moiety, facilitating the sequential construction of intricate molecular structures with high precision and efficiency. Additionally, the tert-Butyl (3-aminocyclopentyl)carbamate hydrochloride can be efficiently cleaved under mild conditions, enabling the facile removal of the protecting group to reveal the free amine functionality in the final product. This strategic use of tert-Butyl (3-aminocyclopentyl)carbamate hydrochloride in chemical synthesis plays a crucial role in the synthesis of diverse bioactive compounds, pharmaceuticals, and functional materials.
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