Skip to Content
Merck
All Photos(1)

Key Documents

678503

Sigma-Aldrich

(+)-Ipc2B(allyl)borane solution

1 M in pentane

Synonym(s):

(+)-Ipc2B(allyl) solution, (+)-B-Allyldiisopinocampheylborane solution

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(C10H17)2BCH2CH=CH2
CAS Number:
Molecular Weight:
326.37
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.22

optical activity

[α]20/D +14°, c = 1 in pentane

Quality Level

concentration

1 M in pentane

bp

35-36 °C

density

0.735 g/mL at 25 °C

storage temp.

−20°C

SMILES string

C[C@@H]1[C@H](C[C@H]2C[C@@H]1C2(C)C)B(CC=C)[C@H]3C[C@H]4C[C@@H]([C@@H]3C)C4(C)C

InChI

1S/C23H39B/c1-8-9-24(20-12-16-10-18(14(20)2)22(16,4)5)21-13-17-11-19(15(21)3)23(17,6)7/h8,14-21H,1,9-13H2,2-7H3/t14-,15-,16+,17+,18-,19-,20-,21-/m0/s1

InChI key

ZIXZBDJFGUIKJS-AXSQLCHVSA-N

Looking for similar products? Visit Product Comparison Guide

General description

http://www.sigmaaldrich.com/ifb/acta/v35/acta-vol35-2002.html#32

Application

This allylboration reagent is a convenient, salt-free, stable solution of a chiral allyl borane for asymmetric allylation of aldehydes leading to chiral homoallylic alcohols.

Other Notes

Material may become hazy upon cooler storage, this will not affect use
Under refrigerator storage, these salt-free, Ipc2B(allyl) reagents do not show any appreciable decrease in selectivity is observed after several months. They exhibit excellent reactivity and reactions can be performed at 5°C, even in water.

Signal Word

Danger

Hazard Classifications

Aquatic Chronic 2 - Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Central nervous system, Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

-56.2 °F

Flash Point(C)

-49 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Total syntheses of epothilones A and B via a macrolactonization-based strategy
Nicolaou KC, et al.
Journal of the American Chemical Society, 119.34, 7974-7991 (1997)
Total synthesis of hyptolide
Chakraborty, Tushar Kanti, and Subhas Purkait.
Tetrahedron Letters, 49.38, 5502-5504 (2008)
Concise total syntheses of epothilone A and C based on alkyne metathesis
Furstner, Alois, Christian Mathes, and Karol Grela.
Chemical Communications (Cambridge, England), 12, 1057-1059 (2001)
Total synthesis of epothilone A: the olefin metathesis approach.
Yang Z, et al.
Angewandte Chemie (International Edition in English), 36(1-2), 166-168 (1997)
Chemoenzymatic synthesis of spinosyn A
Kim, Hak Joong, et al.
Angewandte Chemie (International Edition in English), 53.49, 13553-13557 (2014)

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