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Home > Encyclopedia > Zinc, dibromodi-μ-methylene[μ-(tetrahydrofuran)]tri-, cyclo

Zinc, dibromodi-μ-methylene[μ-(tetrahydrofuran)]tri-, cyclo

Zinc, dibromodi-μ-methylene[μ-(tetrahydrofuran)]tri-, cyclo structure

Zinc, dibromodi-μ-methylene[μ-(tetrahydrofuran)]tri-, cyclo 

structure
  • CAS No:

    41114-59-4

  • Formula:

    C6H12Br2OZn3

  • Chemical Name:

    Zinc, dibromodi-μ-methylene[μ-(tetrahydrofuran)]tri-, cyclo

  • Synonyms:

    Zinc,dibromodi-μ-methylene[μ-(tetrahydrofuran)]tri-,cyclo;Nysted's reagent

Description

The Nysted reagent is a reagent used in organic synthesis for the methenylation of a carbonyl group. It was discovered in 1975 by Leonard N. Nysted in Chicago, Illinois. It was originally prepared by reacting dibromomethane and activated zinc in THF.
A similar reagent is Tebbe's reagent.In the Nysted olefination, the Nysted reagent reacts with TiCl to methylenate a carbonyl group. The biggest problem with these reagents are that the reactivity has not been well documented. It is believed

Zinc, dibromodi-μ-methylene[μ-(tetrahydrofuran)]tri-, cyclo Basic Attributes

456.14

449.712921

Characteristics

9.23000

3.40210

1.186 g/mL at 25ºC(lit.)

−15 °F

Safety Information

UN 3399 4.3/PG 2

3

11-14-19-22-36/37/38-40-36/37

16-26-36-36/37

F,Xn

P210-P280-P305 + P351 + P338-P370 + P378-P403 + P235

H225-H319-H335-H351

Zinc, dibromodi-μ-methylene[μ-(tetrahydrofuran)]tri-, cyclo Use and Manufacturing

Reagent for the methylenation of ketones and aldehydes.

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