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71999-74-1

N-Boc-2-chloroethylamine

Catalog#: AR003SW2  |   CAS#: 71999-74-1  |   MDL#: MFCD04004074  |   MF: C7H14ClNO2  |   MW: 179.6446

Packsize Purity Price Availability Quantity
1g 98% $3.00 Global Stock Buy Now Add To Cart
5g 98% $4.00 Global Stock Buy Now Add To Cart
10g 98% $8.00 Global Stock Buy Now Add To Cart
25g 98% $19.00 Global Stock Buy Now Add To Cart
50g 98% $37.00 Global Stock Buy Now Add To Cart
100g 98% $71.00 Global Stock Buy Now Add To Cart
500g 98% $355.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003SW2
Chemical Name N-Boc-2-chloroethylamine
CAS Number 71999-74-1
Molecular Formula C7H14ClNO2
Molecular Weight 179.6446
MDL Number MFCD04004074
SMILES ClCCNC(=O)OC(C)(C)C

N-Boc-2-chloroethylamine is commonly utilized in chemical synthesis as a versatile building block due to its unique properties and reactivity. This compound is specifically valued for its ability to functionalize molecules with a Boc (tert-butoxycarbonyl) protecting group, a widely used protective group in organic synthesis. The presence of the Boc group not only stabilizes the amine functionality but also enables selective deprotection under mild conditions, making it a valuable tool in the construction of complex organic molecules.In organic synthesis, N-Boc-2-chloroethylamine can serve as an important precursor in the preparation of various compounds, such as amino acids, peptides, pharmaceuticals, and agrochemicals. Its chloroethyl functionality allows for nucleophilic substitution reactions, enabling the introduction of diverse substituents at the amine moiety. Additionally, the Boc protecting group can be selectively removed under acidic conditions, exposing the free amine group for further functionalization or coupling reactions.Furthermore, the versatility of N-Boc-2-chloroethylamine makes it a valuable tool for the modification of biomolecules, such as peptides or proteins, where selective manipulation of functional groups is crucial for studying structure-activity relationships or developing novel bioconjugates. Its ease of handling and compatibility with a wide range of synthetic methods make N-Boc-2-chloroethylamine a valuable building block in modern chemical synthesis strategies.
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