(3R,4R,5S)-Ethyl 4-(N-(tert-butyl)acetamido)-5-(diallylamino)-3-(pentan-3-yloxy)cyclohex-1-enecarboxylate hydrochloride

• CAT Number: L037208
• CAS Number: 651324-08-2
• Molecular Formula: C26H45ClN2O4
• Molecular Weight: 485.10
• Purity: ≥95%
• IUPAC Name: ethyl (3R,4R,5S)-4-[acetyl(tert-butyl)amino]-5-[bis(prop-2-enyl)amino]-3-pentan-3-yloxycyclohexene-1-carboxylate;hydrochloride
• InChI: InChI=1S/C26H44N2O4.ClH/c1-10-15-27(16-11-2)22-17-20(25(30)31-14-5)18-23(32-21(12-3)13-4)24(22)28(19(6)29)26(7,8)9;/h10-11,18,21-24H,1-2,12-17H2,3-9H3;1H/t22-,23+,24+;/m0./s1
• InChIKey: PUBKCMTVXFIUCX-BAUONJEJSA-N
• SMILES: CCC(CC)O[C@@H]1C=C(C[C@@H]([C@H]1N(C(=O)C)C(C)(C)C)N(CC=C)CC=C)C(=O)OCC.Cl

(3R,4R,5S)-Ethyl 4-(N-(tert-butyl)acetamido)-5-(diallylamino)-3-(pentan-3-yloxy)cyclohex-1-enecarboxylate hydrochloride（Cat No.:L037208）is a complex, chiral cyclohexene derivative used as an intermediate in medicinal and synthetic organic chemistry. It features multiple functional groups, including an ethyl ester, a tert-butyl-protected acetamido group, a diallylamino substituent, and a pentan-3-yloxy ether, contributing to its versatility in drug discovery and development. The hydrochloride salt enhances solubility and stability. Its stereochemically defined cyclohexene ring allows for selective interaction with biological targets, making it valuable in the synthesis of bioactive molecules or pharmacologically relevant compounds. Store in a dry, controlled environment.