This compound is a highly functionalized, chiral boron-containing heterocycle, present as a trifluoroacetate salt (1:1). Structurally, it features a benzodioxaborole core, a primary amine side chain, and multiple stereogenic centers, indicating deliberate asymmetric synthesis. The boron heterocycle and protected, rigid bicyclic framework are characteristic of advanced synthetic building blocks used in medicinal chemistry and complex API synthesis, particularly where enzyme binding, stereochemical precision, or boron-based pharmacophores are required. The directory classifies it as a under development API with a synthetic source/manufacturing origin. Other names for this substance include Bortezomib Impurity 38 and (R)-BoroLeu-(+)-pinanediol-trifluoroacetate. Its PubChem CID is 44244713.
4,6-Methano-1,3,2-benzodioxaborole-2-methanamine, hexahydro-3a,8,8-trimethyl-alpha-(2-methylpropyl)-, (alphaR,3aS,4S,6S,7aR)-, 2,2,2-trifluoroacetate (1:1)
| CAS No | 179324-87-9 |
|---|---|
| Molecular Formula | C17H29BF3NO4 |
| Molecular Weight | 379.2 g/mol |
| Synonyms | (1R)-3-methyl-1-[(1S,2S,6R,8S)-2,9,9-trimethyl-3,5-dioxa-4-boratricyclo[6.1.1.02,6]decan-4-yl]butan-1-amine;2,2,2-trifluoroacetic acid |
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Frequently Asked Questions
This compound is a highly functionalized, chiral boron-containing heterocycle, present as a trifluoroacetate salt (1:1). Structurally, it features a benzodioxaborole core, a primary amine side chain, and multiple stereogenic centers, indicating deliberate asymmetric synthesis.
The listed CAS number is 179324-87-9.
The listed molecular formula is C17H29BF3NO4.
The listed molecular weight is 379.2 g/mol.
(1R)-3-methyl-1-[(1S,2S,6R,8S)-2,9,9-trimethyl-3,5-dioxa-4-boratricyclo[6.1.1.02,6]decan-4-yl]butan-1-amine;2,2,2-trifluoroacetic acid.
The source lists Bortezomib Impurity 38 and (R)-BoroLeu-(+)-pinanediol-trifluoroacetate.