Compound Q&A
How is N-Cyclohexylcyclohexanamine - 5-bromo-4-chloro-1H-indol-3-yl beta-D-glucopyranosiduronic acid (1:1) (CAS: 18656-96-7) typically synthesized?
Answer
N-Cyclohexylcyclohexanamine - 5-bromo-4-chloro-1H-indol-3-yl beta-D-glucopyranosiduronic acid (1:1) is synthesized through a multi-step process involving the coupling of indol-3-yl beta-D-glucopyranosiduronic acid with N-cyclohexylcyclohexanamine and subsequent bromination and chlorination reactions. The synthesis typically requires the use of catalysts such as aluminum chloride and phosphorus pentoxide, and the process yields up to 85% of the desired compound under optimized conditions.
About
CAS No
18656-96-7
English Name
N-Cyclohexylcyclohexanamine - 5-bromo-4-chloro-1H-indol-3-yl beta-D-glucopyranosiduronic acid (1:1)
Molecular Formula
C26H36BrClN2O7
Molecular Weight
521.79 g/mol
EINECS
239-603-0
SMILES
[O-]C(=O)[C@H]1O[C@@H](Oc2c[nH]c3c2c(Cl)c(cc3)Br)[C@@H]([C@H]([C@@H]1O)O)O.[NH3+]C1CCCCC1
InChIKey
GKUBHKZCDXMPME-CYRSAHDMSA-N
Last Updated: 2025-10-01 13:51
