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AJ16577

1049743-64-7 | Boc-1,3-cis-damch hcl

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $112.00 $78.00 -   +
1g 95% in stock $189.00 $132.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AJ16577
Chemical Name: Boc-1,3-cis-damch hcl
CAS Number: 1049743-64-7
Molecular Formula: C13H27ClN2O2
Molecular Weight: 278.8187
MDL Number: MFCD04973128
SMILES: NC[C@H]1CCC[C@H](C1)CNC(=O)OC(C)(C)C.Cl

 

Upstream Synthesis Route
  • Boc-1,3-cis-damch hcl, a versatile chemical compound widely utilized in organic synthesis, plays a crucial role in various chemical reactions due to its unique properties. This compound, possessing a Boc (tert-butoxycarbonyl) group and a 1,3-cis configuration, is particularly valuable in the protection of amines during synthetic processes. By selectively masking the amino group with the Boc protecting group, Boc-1,3-cis-damch hcl helps prevent unwanted reactions and enables precise control over the reaction conditions.In chemical synthesis, Boc-1,3-cis-damch hcl serves as a key building block in the creation of complex organic molecules. Its ability to protect amines allows chemists to carry out reactions at specific sites within a molecule, thereby facilitating the synthesis of structurally diverse compounds. Additionally, the Boc group can be easily removed under mild conditions, providing access to the desired amine functionality at later stages of the synthesis.Overall, the application of Boc-1,3-cis-damch hcl in chemical synthesis enables chemists to manipulate and transform organic molecules with precision, opening up avenues for the creation of new drugs, materials, and other valuable compounds.
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