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AE08830

108999-93-5 | cis-4-((tert-Butoxycarbonyl)amino)cyclopent-2-enecarboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $9.00 $6.00 -   +
250mg 95% in stock $18.00 $12.00 -   +
1g 95% in stock $63.00 $44.00 -   +
5g 95% in stock $290.00 $203.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE08830
Chemical Name: cis-4-((tert-Butoxycarbonyl)amino)cyclopent-2-enecarboxylic acid
CAS Number: 108999-93-5
Molecular Formula: C42H66N2O16
Molecular Weight: 854.9772
MDL Number: MFCD00211287
SMILES: O=C(C(C(OC(=O)C(=O)OC(C)(C)C)(C)C)N[C@H]1C=C[C@H](C1)C(=O)O)OC(C)(C)C.O=C(C(C(OC(=O)C(=O)OC(C)(C)C)(C)C)N[C@@H]1C=C[C@@H](C1)C(=O)O)OC(C)(C)C

 

Upstream Synthesis Route
  • Cis-4-((tert-Butoxycarbonyl)amino)cyclopent-2-enecarboxylic acid, or $name$, is a versatile compound commonly used in chemical synthesis. Its unique structure allows it to participate in a variety of reactions and serve as a key building block in the creation of complex molecules.One of the main applications of $name$ in chemical synthesis is as a protecting group for the amino functionality. By adding the tert-Butoxycarbonyl (Boc) group to the amino group, $name$ can shield the amine from unwanted reactions during the synthetic process. This protection is essential in multi-step syntheses where selective reactions are crucial for success.Additionally, $name$ can be utilized in the formation of peptide bonds. The presence of the Boc protecting group allows for controlled deprotection under specific conditions, enabling the coupling of amino acids to form peptides and proteins.Furthermore, $name$ can also be employed in the synthesis of pharmaceuticals, agrochemicals, and other valuable compounds where precise control over functional groups is necessary for the desired outcome. Its role as a versatile intermediate highlights its importance in modern organic chemistry and drug discovery efforts.
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