Dibromochloromethane, 97+%, Thermo Scientific Chemicals
Dibromochloromethane, 97+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Dibromochloromethane, 97+%, Thermo Scientific Chemicals

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Quantity:
25 g
5 g
100 g
Catalog number A16938.14
also known as A16938-14
Price (USD)/ Each
106.00
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Quantity:
25 g
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Price (USD)/ Each
106.00
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Dibromochloromethane, 97+%, Thermo Scientific Chemicals
Catalog numberA16938.14
Price (USD)/ Each
106.00
-
Add to cart
Chemical Identifiers
CAS124-48-1
IUPAC Namedibromo(chloro)methane
Molecular FormulaCHBr2Cl
InChI KeyGATVIKZLVQHOMN-UHFFFAOYSA-N
SMILESClC(Br)Br
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥97.0%
FormLiquid
Refractive Index1.5455-1.5495 @ 20?C
Appearance (Color)Clear colorless to yellow
It affords bromochlorocarbene under phase-transfer conditions.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It affords bromochlorocarbene under phase-transfer conditions.

Solubility
Not miscible or difficult to mix in water.

Notes
Moisture & Light Sensitive. Store away from light, water/moisture, oxidizing agents and heat. Store under inert gas.
RUO – Research Use Only

General References:

  1. M. Fedoryński.; M. Popławska.; K. Nitschke.; W. Kowalski & M. Mâkosza. A Simple Method for Preparation of Dibromochloromethane and Bromodichloromethane.An International Journal for Rapid Communication of Synthetic Organic Chemistry.,1977,7(4), 287-292.
  2. Y. Yokouchi1.; F. Hasebe.; M. Fujiwara.; H. Takashima.; M. Shiotani.; N. Nishi.; Y. Kanaya.; S. Hashimoto.; P. Fraser.; D. Toom-Sauntry.; H. Mukai.; and Y. Nojiri. Correlations and emission ratios among bromoform, dibromochloromethane, and dibromomethane in the atmosphere.Journal of Geophysical Research: Atmospheres .,2005,110(D23).
  3. Source of bromochlorocarbene in the presence of base and Dibenzo-18-crown-6, A13133. Other conditions give mixtures of carbenes: Synthesis, 783 (1977); Tetrahedron, 33, 363 (1977).