Skip to Content
MilliporeSigma
All Photos(1)

Documents

237701

Sigma-Aldrich

S-Alpine-Borane® solution

0.5 M in THF

Synonym(s):

B-isopinocampheyl-9-borabicyclo[3.3.1]nonane

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C18H31B
CAS Number:
42371-63-1
Molecular Weight:
258.25
MDL number:
MFCD00082390
UNSPSC Code:
12352000
PubChem Substance ID:
24854265
NACRES:
NA.22

form

liquid

optical activity

[α]22/D +1.2°, neat

concentration

0.5 M in THF

density

0.897 g/mL at 25 °C

SMILES string

C[C@@H]1[C@H](C[C@H]2C[C@@H]1C2(C)C)B3[C@@H]4CCC[C@H]3CCC4

InChI

1S/C18H31B/c1-12-16-10-13(18(16,2)3)11-17(12)19-14-6-4-7-15(19)9-5-8-14/h12-17H,4-11H2,1-3H3/t12-,13+,14-,15+,16-,17-/m0/s1

InChI key

VCDGSBJCRYTLNU-NEXGVSGLSA-N

General description

S-Alpine-Borane® is a chiral reducing agent, synthesized from (-)-α-pinene via hydroboration.

Application

R- and S-Alpine-Boranes are used for asymmetric reduction of aldehydes and prochiral ketones.
S-Alpine-Borane® solution may be used to prepare:
  • 5(S)-methyl 5-hydroxy-8-(tetrahydropyran-2-yloxy)-6-octynoate, an intermediate for the stereocontrolled total synthesis of leukotriene B4.
  • (+)-(S)-4-hydroxy-6-phenyl-5-hexynyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carboxylate
  • (R)-1-(tert-Butyldiphenylsilyloxy)pent-3-yn-2-ol, an intermediate for the preparation of (S)-4,5-dihydroxypentane-2,3-dione (DPD).

Legal Information

Alpine-Borane is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - Pyr. Liq. 1 - STOT SE 3

target_organs

Respiratory system

supp_hazards

EUH019

Storage Class

4.2 - Pyrophoric and self-heating hazardous materials

wgk_germany

WGK 3

flash_point_f

1.4 °F - closed cup

flash_point_c

-17 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

(-)-Sparteine-Mediated Stereoselective Intramolecular Carbolithiation of 4-Substituted 5-Hexynyl Carbamates. Synthesis of Enantiopure 1, 3-Difunctionalized Alkylidene Cyclopentanes.
Oestreich M, et al.
The Journal of Organic Chemistry, 64(23), 8616-8626 (1999)
An efficient synthesis of the precursor of AI-2, the signalling molecule for inter-species quorum sensing.
Ascenso OS, et al.
Bioorganic & Medicinal Chemistry, 19(3), 1236-1241 (2011)
Tetrahedron Asymmetry, 5, 1061-1061 (1994)
Total synthesis of leukotriene B4.
Kerdesky FAJ, et al.
The Journal of Organic Chemistry, 58(13), 3516-3520 (1993)
Aldrichimica Acta, 15, 68-68 (1982)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service