762-67-4

Basic information

• Product Name: ALLYLTRICHLOROGERMANE
• Synonyms: ALLYLTRICHLOROGERMANE;ALLYTRICHLOROGERMANE
• CAS NO: 762-67-4
• Molecular Formula: C₃H₅Cl₃Ge
• Molecular Weight: 220.07
• Mol File: 762-67-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 154-7°C
• Flash Point: 55°C
• Appearance: /
• Density: 1,527 g/cm3
• Vapor Pressure: 4.76mmHg at 25°C
• Refractive Index: 1.4928
• CAS DataBase Reference: ALLYLTRICHLOROGERMANE(CAS DataBase Reference)
• NIST Chemistry Reference: ALLYLTRICHLOROGERMANE(762-67-4)
• EPA Substance Registry System: ALLYLTRICHLOROGERMANE(762-67-4)

Safety Data

• TSCA: No
• Hazardous Substances Data: 762-67-4(Hazardous Substances Data)

Usage

Description

Allyl trichlorogermane, with the chemical formula C3H5GeCl3, is a colorless liquid characterized by a pungent odor. It functions as a Lewis acid, enabling it to form coordination complexes with a variety of organic substrates. ALLYLTRICHLOROGERMANE is primarily utilized as a reagent in organic synthesis and has potential applications in the development of germanium-based materials and technologies. However, it is essential to handle allyl trichlorogermane with care due to its toxic nature and its classification as a hazardous substance, which poses potential risks to both human health and the environment.

Uses

Used in Organic Synthesis:
Allyl trichlorogermane is used as a reagent in organic synthesis for its ability to form coordination complexes with organic substrates, facilitating various chemical reactions and the synthesis of new compounds.
Used in Material Science:
In the field of material science, allyl trichlorogermane is utilized for its potential role in the production of germanium-based materials, which can be applied in various technological advancements.
Used in Research and Development:
Due to its unique properties as a Lewis acid, allyl trichlorogermane is also employed in research and development settings to explore new methods and applications in chemical processes and material innovations.

InChI:InChI=1/C3H5Cl3Ge/c1-2-3-7(4,5)6/h2H,1,3H2

Upstream product

• 1074-29-9 trichlorophenylgermane 
• 107-05-1 3-chloroprop-1-ene 
• 7440-56-4 germanium 
• 13465-77-5 hexachlorodisilane 
• 10038-98-9 germaniumtetrachloride 
• 7647-01-0 hydrogenchloride 

Relevant articles and documents

Organotrichlorogermane synthesis by the reaction of elemental germanium, tetrachlorogermane and organic chloride via dichlorogermylene intermediate

Organotrichlorogermanes were synthesized by the reaction of elemental germanium, tetrachlorogermane and organic chlorides, methyl, propyl, isopropyl and allyl chlorides. Dichlorogermylene formed by the reaction of elemental germanium with tetrachlorogermane was the reaction intermediate, which was inserted into the carbon-chlorine bond of the organic chloride to give organotrichlorogermane. When isopropyl or allyl chloride was used as an organic chloride, organotrichlorogermane was formed also in the absence of tetrachlorogermane. These chlorides were converted to hydrogen chloride, which subsequently reacted with elemental germanium to give the dichlorogermylene intermediate. The reaction of elemental germanium, tetrachlorogermane and organic chlorides provides a simple and easy method for synthesizing organotrichlorogermanes, and all the raw materials are easily available.

Thermal transformations of phenyltrichlorogermane in the gas phase

Pyrolysis of PhGeCl3 and its mixtures with allyl chloride and isoprene in the temperature range 500-680°C was investigated. PhGeCl3 vigorously decomposes at temperatures higher 600°C, and its decomposition involves both dichlorogermylenes and trichlorogermyl radical. Pyrolysis of mixtures of PhGeCl3 with isoprene or allyl chloride yields respectively trichloro(1,2-dimethyl-2-propenyl)germane, isopentyltrichloro germanes, and 1,1-dichloro-3-methyl-1-germacyclo-3-pentene or allyltrichlorogermane. A mechanism of formation of these products is proposed.