C20H34BCl
320.7 g/mol
Research ReagentDanger
Chlorobis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]borane
CAS112246-73-8
Category
Research Reagent
Compound Class
Organometallic
Primary Use
Research Compound
This compound is an asymmetric reducing agent and chiral reagent used in organic synthesis. It is a chloroborane derivative with two chiral bicyclic groups, designed for enantioselective reductions in research and laboratory settings.
asymmetric reducing agentchiral reagent for enantioselective synthesislaboratory research reagent
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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CAS 112246-73-8
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Referencestereoisomer of
(-)-Diisopinocampheyl chloroborane
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Safety Reference
Danger
H314Causes severe skin burns and eye damage
H318Causes serious eye damage
Identifiers
IUPAC Name
chloro-bis[(1S,2R,3S,5S)-2,6,6-trimethyl-3-bicyclo[3.1.1]heptanyl]borane
InChIKey
PSEHHVRCDVOTID-NAVXHOJHSA-N
SMILES
B([C@H]1C[C@H]2C[C@@H]([C@@H]1C)C2(C)C)([C@H]3C[C@H]4C[C@@H]([C@@H]3C)C4(C)C)Cl
Synonyms (7)
- (+)-DIP-Chloride