3-Chloro-2-methylpropene CAS 563-47-3-liquid-2

3-Chloro-2-methylpropene CAS 563-47-3-liquid-4

3-Chloro-2-methylpropene CAS 563-47-3-liquid-3

3-Chloro-2-methylpropene CAS 563-47-3

CAS: 563-47-3
Molecular Formula: C4H7Cl
Molecular Weight: 90.55
EINECS: 209-251-2
Tiempo de almacenamiento: 2 años

Synonyms: beta-Methylallyl chloride; beta-methylallylchloride; chloruedemethallyle(french); Chlorure de methallyle; chloruredemethallyle; chloruredemethallyle(french); Cloruro di metallile;clorurodimetallile

What is 3-Chloro-2-methylpropene CAS 563-47-3 ?

3-Chloro-2-methylpropene CAS 563-47-3 is a colorless transparent liquid with pungent odor, insoluble in water, soluble in ethanol, ethyl ether, acetone and other organic solvents.

Especificación

Artículos de la prueba	Estándar
Punto de fusión	-80 °C (lit.)
Punto de ebullición	71-72 °C (lit.)
Densidad	0.925 g/mL at 20 °C (lit.)
Apariencia	líquido incoloro transparente

Aplicación

3-chloro-2-methylpropene, an important intermediate in organic synthesis, has a wide range of applications in many fields：

Campo farmacéutico: can be used to synthesize a variety of drugs. It is a key intermediate in the synthesis of certain antibacterial drugs, and through a series of chemical reactions, it can introduce specific functional groups to build a drug molecular structure with antibacterial activity.

Pesticide field: It is an important raw material for the synthesis of new pesticides. It can participate in the preparation of pesticide ingredients with efficient insecticidal, bactericidal or herbicidal activity, which helps to improve the yield and quality of crops and reduce the damage of diseases and pests to crops.

Fragrance industry: plays an important role in fragrance synthesis. Chemical reactions can produce compounds with special fragrances, which can be used to prepare various flavors to add unique aromas to perfumes, cosmetics, food, etc.

Field of organic synthesis: As a key reagent in organic synthesis, it can be used to construct complex organic molecular structures. It can react with a variety of reagents, such as substituting with compounds containing active hydrogen, introducing allyl chloride groups, providing rich possibilities for subsequent synthetic reactions, and is widely used in the synthesis of fine chemical products.