Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

555959

Sigma-Aldrich

Dichloroborane dioxane complex solution

3 M in methylene chloride

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
C4H8O2 · BHCl2
CAS Number:
252265-33-1
Molecular Weight:
170.83
MDL number:
MFCD03427168
UNSPSC Code:
12352005
PubChem Substance ID:
24879506
NACRES:
NA.22

reaction suitability

reagent type: reductant

Quality Level

100

concentration

3 M in methylene chloride

density

1.321 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

Cl[BH-](Cl)[O+]1CCOCC1

InChI

1S/C4H9BCl2O2/c6-5(7)9-3-1-8-2-4-9/h5H,1-4H2

InChI key

RCKKTUSYECYDLY-UHFFFAOYSA-N

Related Categories

Application

Reactant for:
  • Hydroboration reactions
  • Preparation of alkenyl- and alkylboronic acids
Can readily substitute for common hydroborating reagents such as BH3 · THF and BMS.

Legal Information

U.S. Pat. No. 6,008,414

Signal Word

Danger

Hazard Statements

H314,H336,H351

Hazard Classifications

Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

Target Organs

Central nervous system

Supplementary Hazards

EUH014

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

221.0 °F - closed cup

Flash Point(C)

105 °C - closed cup

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

J V Kanth et al.
The Journal of organic chemistry, 66(16), 5359-5365 (2001-08-04)
Several less volatile oxygen-containing Lewis bases, such as tert-butyl methyl ether, dioxane, anisole, ethyl acetate, beta-chloroethyl ether, and monoglyme, were examined as prospective mono- and dichloroborane carriers. Dioxane, ethyl acetate, and beta-chloroethyl ether form relatively stable boron trichloride adducts, but
Kanth, J. V. B.; Brown, H. C.
Organic Letters, 1, 315-315 (1999)
Josyula, K. V. B. et al
Tetrahedron Letters, 44, 7789-7789 (2003)

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