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(-)-Isopinocampheylborane TMEDA Complex

Catalog Number
ACM67826920-1
Product Name
(-)-Isopinocampheylborane TMEDA Complex
Structure
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CAS
67826-92-0
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Synonyms
I0796; (-)-Isopinocampheylborane TMEDA complex; (S)-(+)-Alpine-Boramine; (-)-N,N inverted exclamation marka-Bis(monoisopinocampheylborane)-N,N,N inverted exclamation marka,N inverted exclamation marka-tetramethylethylenediamine; CA-1091; 67826-92-0; MFCD00077801;
IUPAC Name
N,N,N',N'-tetramethylethane-1,2-diamine;[(1S,2R,3S,5S)-2,6,6-trimethyl-3-bicyclo[3.1.1]heptanyl]boron;
Molecular Weight
412.32g/mol
Molecular Formula
C26H50B2N2;
Canonical SMILES
[B]C1CC2CC(C1C)C2(C)C.[B]C1CC2CC(C1C)C2(C)C.CN(C)CCN(C)C;
InChI
InChI=1S/2C10H17B.C6H16N2/c2*1-6-8-4-7(5-9(6)11)10(8,2)3;1-7(2)5-6-8(3)4/h2*6-9H,4-5H2,1-3H3;5-6H2,1-4H3/t2*6-,7+,8-,9-;/m00./s1;
InChI Key
YIPGSNPACSKQKJ-NCHGFZPDSA-N;
Storage
2-8°C
Complexity
216
Covalently-Bonded Unit Count
3
Defined Atom Stereocenter Count
8
Exact Mass
412.416g/mol
H-Bond Acceptor
2
Heavy Atom Count
30
Monoisotopic Mass
412.416g/mol
Rotatable Bond Count
3
Topological Polar Surface Area
6.5A^2
Application
The (-)-Isopinocampheylborane TMEDA Complex is designed as a chiral hydroboration reagent, playing a crucial role as a polarity-reversal catalyst. Its main application lies in the kinetic resolution of racemic esters and ketones, thereby facilitating the selective transformation of these compounds.
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