ରଙ୍ଗହୀନ ତରଳ ହାଲୋଫର୍ମ CHBr3 |,

bromoform's Usage Examples:

be used to transform acetyl groups into carboxyl groups or to produce chloroform (CHCl3), bromoform (CHBr3), or iodoform (CHI3).

This page provides supplementary chemical data on bromoform.

The oceans are estimated to release 1–2 million tons of bromoform and 56,000 tons of bromomethane annually.

limits the total concentration of the four chief constituents (chloroform, bromoform, bromodichloromethane, and dibromochloromethane), referred to as total.

acetyl groups into carboxyl groups or to produce chloroform (CHCl3), bromoform (CHBr3), or iodoform (CHI3).

The essential oil of limu kohu is 80% bromoform (tri-bromo-methane) by weight, and includes many other bromine- and iodine-containing.

bromination leads to the formation of bromoform.

(Muthmanns solution), potassium tetraiodomercurate(II) (Thoulets solution), bromoform or diiodomethane which are used in mineralogy are very toxic.

Carbenes derived from chloroform or bromoform can be used to add CX2 to an alkene to give a dihalocyclopropane, while the Simmons–Smith reagent adds CH2.

In the original reaction, the organochromium species is generated from iodoform or bromoform and an excess of chromium(II) chloride and the product is.

The vanadium bromoperoxidases produce an estimated 1–2 million tons of bromoform and 56,000 tons of bromomethane.

The compound is prepared by the reaction of dicobalt octacarbonyl with bromoform.

Liquids used include bromoform, tetrabromoethane, tribromoethane, methylene iodide, and polytungstate.