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1,3-Dioxolane,4-[(1Z)-4,4-dichloro-1,3-butadienyl]-2,2-dimethyl-,(4S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

804482-74-4

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804482-74-4 Usage

Appearance

Colorless liquid
The compound is a colorless liquid at room temperature.

Molecular weight

231.12 g/mol
The molecular weight of the compound is 231.12 grams per mole.

Industrial applications

Chemical intermediate in the production of pharmaceuticals, agrochemicals, and fragrances
The compound is used as a starting material for the synthesis of various products in different industries.

Hazardous properties

a. Harmful if swallowed
Ingestion of the compound can cause harm to the body.
b. Causes skin and eye irritation
Contact with the skin or eyes can result in irritation.
c. May cause respiratory tract irritation if inhaled
Inhalation of the compound's vapors or dust can lead to respiratory irritation.

Environmental impact

Harmful to aquatic life and can cause long-term adverse effects in the aquatic environment
The compound poses a risk to aquatic organisms and ecosystems, and its release into water bodies should be avoided.

Check Digit Verification of cas no

The CAS Registry Mumber 804482-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,4,4,8 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 804482-74:
(8*8)+(7*0)+(6*4)+(5*4)+(4*8)+(3*2)+(2*7)+(1*4)=164
164 % 10 = 4
So 804482-74-4 is a valid CAS Registry Number.

804482-74-4Downstream Products

804482-74-4Relevant academic research and scientific papers

3,3,3-Trichloropropyl-1-triphenylphosphorane: A reagent for the synthesis of (Z)-1,3-enynes, (Z,Z)-1-chloro-1,3-dienes, and 1,3-diynes

Karatholuvhu, Maheswaran S.,Fuchs, Philip L.

, p. 14314 - 14315 (2004)

,3,3,3-Trichloropropyl-1-triphenylphosphonium chloride is conveniently prepared from 2-chloroethanol, triphenylphosphine, and trichloroacetic acid. Deprotonation of this reagent generates 3,3,3-trichloropropyl-1-triphenylphosphorane, which reacts with aldehydes to give trichloromethylated (Z)-olefins, which are useful for the synthesis of (Z)-1,3-enynes, (Z,Z)-1-chloro-1,3-dienes, and 1,3-diynes in high yields and stereospecificities. Copyright

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