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Home  > (2S)-(6aR,11aR,11bS)-4,4,6a,7,11b-Pentamethyl-2,3,4,4a,5,6,6a,11,11a,11b-decahydro-1H-benzo[a]fluoren-9-yl 2,6-diaminohexanoate

AA00090

1000010-11-6 | (2S)-(6aR,11aR,11bS)-4,4,6a,7,11b-Pentamethyl-2,3,4,4a,5,6,6a,11,11a,11b-decahydro-1H-benzo[a]fluoren-9-yl 2,6-diaminohexanoate

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Description
Catalog Number: AA00090
Chemical Name: (2S)-(6aR,11aR,11bS)-4,4,6a,7,11b-Pentamethyl-2,3,4,4a,5,6,6a,11,11a,11b-decahydro-1H-benzo[a]fluoren-9-yl 2,6-diaminohexanoate
CAS Number: 1000010-11-6
Molecular Formula: C28H46Cl2N2O2
Molecular Weight: 513.583
MDL Number: MFCD22419382
SMILES: NCCCC[C@@H](C(=O)Oc1cc(C)c2c(c1)C[C@H]1[C@@]2(C)CC[C@@H]2[C@]1(C)CCCC2(C)C)N.Cl.Cl

 

Upstream Synthesis Route
  • The compound (2S)-(6aR,11aR,11bS)-4,4,6a,7,11b-Pentamethyl-2,3,4,4a,5,6,6a,11,11a,11b-decahydro-1H-benzo[a]fluoren-9-yl 2,6-diaminohexanoate serves as a valuable building block in chemical synthesis due to its unique structure and reactivity. It can be employed as a chiral starting material for the synthesis of complex molecules, particularly in the formation of chiral amine derivatives. This compound's stereochemistry and substitution pattern make it a versatile precursor for the creation of diverse chemical structures with specific spatial arrangements. In chemical synthesis, it can act as a key intermediate in the construction of pharmaceuticals, agrochemicals, and materials with tailored properties. The incorporation of this compound enables the introduction of chirality while maintaining a high degree of control over the overall molecular architecture.
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