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317039

Sigma-Aldrich

(+)-B-Methoxydiisopinocampheylborane

Synonym(s):

(+)-Diisopinocampheylmethoxyborane

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About This Item

Empirical Formula (Hill Notation):
C21H37BO
CAS Number:
Molecular Weight:
316.33
Beilstein:
6370228
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.22

form

solid

SMILES string

COB([C@H]1CC2CC([C@@H]1C)C2(C)C)[C@H]3CC4CC([C@@H]3C)C4(C)C

InChI

1S/C21H37BO/c1-12-16-8-14(20(16,3)4)10-18(12)22(23-7)19-11-15-9-17(13(19)2)21(15,5)6/h12-19H,8-11H2,1-7H3/t12-,13-,14+,15+,16-,17-,18-,19-/m0/s1

InChI key

IAQXEQYLQNNXJC-JPDDNCELSA-N

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Application

Reactant involved in:
  • Oxidative cyclization and alkylation for synthesis of ionomycin
  • Intramolecular conjugate addition for tetrahydropyran synthesis
  • Aldol addition and Suzuki coupling reactions
  • Allylation
  • Synthesis of alkanols
Both (+)- and (-)-forms are precursors to B-allyldiisopinocampheylborane derivatives, which are subsequently reacted with aldehydes to give homoallylic alcohols and β-amino alcohols of high enantiomeric excess.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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The Journal of Organic Chemistry, 56, 401-401 (1991)
Journal of the Chemical Society. Chemical Communications, 339-339 (1993)
Aldrichimica Acta, 20, 9-9 (1987)

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