10061-02-6 Usage
Description
(E)-1,3-Dichloro-1-propene, also known as 1,3-Dichloropropene or Telone, is a colorless to pale yellow liquid chemical compound with a variety of applications in agriculture and chemical manufacturing. It is recognized for its effectiveness in controlling pests and pathogens in agricultural settings, as well as its role in the production of other chemicals, polymers, and pesticides. However, due to its hazardous nature, it is essential to handle and use this chemical with caution, taking proper safety measures to prevent skin and eye irritation and toxic effects from ingestion or inhalation.
Uses
Used in Agricultural Industry:
(E)-1,3-Dichloro-1-propene is used as a soil fumigant for controlling pests and pathogens in agricultural settings. It is effective in protecting crops from various soil-borne diseases and pests, thereby ensuring a healthy and productive agricultural yield.
Used in Chemical Manufacturing:
(E)-1,3-Dichloro-1-propene is used as a key component in the production of other chemicals, polymers, and pesticides. Its versatility in chemical synthesis allows for the creation of a wide range of products that serve various purposes in different industries.
Used in Pesticide Production:
(E)-1,3-Dichloro-1-propene is used as an active ingredient in the formulation of pesticides. Its ability to control pests and pathogens makes it a valuable component in the development of effective and efficient pest control solutions for agricultural and other applications.
Check Digit Verification of cas no
The CAS Registry Mumber 10061-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,6 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10061-02:
(7*1)+(6*0)+(5*0)+(4*6)+(3*1)+(2*0)+(1*2)=36
36 % 10 = 6
So 10061-02-6 is a valid CAS Registry Number.
InChI:InChI=1/C3H4Cl2/c4-2-1-3-5/h1-2H,3H2/b2-1+
10061-02-6Relevant articles and documents
Reaction of trifluoromethylsulfenyl chloride with 3-chloro- and 3-hydroxypropynes
Munavalli,Rohrbaugh,Rossman,Berg,Durst
, p. 1645 - 1655 (2004)
Vinylsulfides are often obtained via the reaction of substituted acetylenes with sulfur-containing reagents. The presence of other functional groups such as the halide or the hydroxyl moieties enhances the usefulness of the vinylsulfide intermediates. To this end, propargyl alcohol and halides have found wide application. With a view to enhance the biological properties of the end products synthesized from the vinylsulfide intermediates, the trifluoromethylthio function has now been incorporated as a part of the vinylic system. This communication presents the free-radical addition of trifluoromethyl-sulfenyl chloride to 3-chloro- and 3-hydroxypropynes, and the mechanism of the formation of the various products and their spectral characterization.
MANUFACTURE OF DICHLOROPROPANOL
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Page/Page column 19-21, (2009/03/07)
Manufacture of dichloropropanol Process for manufacturing dichloropropa nol wherein a glycerol-based product comprising at least one diol containi ng at least 3 carbon atoms other than 1,2- propanediol, is reacted with a chlorinati ng agent, and of products derived from dichloropropanol such as ep ichlorohydrin and epoxy resins. No figure.