Skip to Content
Merck
All Photos(1)

Documents

225762

Sigma-Aldrich

Catecholborane solution

1.0 M in THF

Synonym(s):

Catecholatoborane, Catecholborane (CB), Pyrocatecholborane

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C6H5BO2
CAS Number:
Molecular Weight:
119.91
Beilstein:
972072
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

form

liquid

Quality Level

reaction suitability

reagent type: reductant

concentration

1.0 M in THF

density

0.958 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

[bH]1oc2ccccc2o1

InChI

1S/C6H5BO2/c1-2-4-6-5(3-1)8-7-9-6/h1-4,7H

InChI key

CENMEJUYOOMFFZ-UHFFFAOYSA-N

Application

Catecholborane solution can be used as a reducing agent in the Ti-catalyzed reduction of aromatic ketones to alcohols. It can also be used as a reagent for the hydroboration of diene/triene compounds.

Legal Information

Made under U.S. Pat. No. 6,204,405.

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

Target Organs

Central nervous system, Respiratory system

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

1.4 °F - closed cup

Flash Point(C)

-17 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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

Synthetic Communications, 24, 1019-1019 (1994)
Asymmetric Reduction of Ketones with Catecholborane Using 2, 6-BODOL Complexes of Titanium (IV) as Catalysts
Sarvary I, et al.
Chemistry?A European Journal , 7, 2158-2166 (2001)
Journal of the Chemical Society. Chemical Communications, 1673-1673 (1993)
New synthetic strategy targeting well-defined alpha, omega-telechelic polymethylenes with hetero bi-/tri-functionalities via polyhomologation of ylides initiated by new organic boranes based on catecholborane and post functionalization
Xu F, et al.
Royal Society of Chemistry Advances, 6, 69828-69835 (2016)
Chemical Reviews, 91, 1179-1179 (1991)

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