6795-75-1 Usage
Uses
Used in Chemical Synthesis:
1,2-Dichlorobromoethene is used as a chemical intermediate for the production of flame retardants, plastics, and resins. Its unique chemical properties make it a valuable component in the synthesis of these materials, contributing to their flame retardant and plasticizing characteristics.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 1,2-Dichlorobromoethene is used as a key intermediate in the synthesis of various organic compounds, including pharmaceuticals. Its reactivity and versatility in chemical reactions allow for the creation of a wide range of medicinal compounds.
Used in Agricultural Chemical Synthesis:
Similarly, in the agricultural chemical sector, 1,2-Dichlorobromoethene is utilized as an intermediate in the synthesis of various compounds, such as pesticides and herbicides. Its role in these applications is crucial for the development of effective and efficient agricultural products.
Used as a Solvent:
Due to its solvent properties, 1,2-Dichlorobromoethene is also employed in various industrial processes where its ability to dissolve other substances is required. This use is particularly relevant in the manufacturing of certain types of products where specific solubility characteristics are needed.
Check Digit Verification of cas no
The CAS Registry Mumber 6795-75-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,9 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6795-75:
(6*6)+(5*7)+(4*9)+(3*5)+(2*7)+(1*5)=141
141 % 10 = 1
So 6795-75-1 is a valid CAS Registry Number.
InChI:InChI=1/C2HBrCl2/c3-2(5)1-4/h1H/b2-1+
6795-75-1Relevant articles and documents
Intramolecular Geminal and Vicinal Element Effects in Substitution of Simple Bromo(chloro)alkenes by Methoxide and Thiolate Ions. An Example of a Single Step Substitution?
Beit-Yannai, Michal,Rappoport, Zvi,Shainyan, Bagrat A.,Danilevich, Yuri S.
, p. 8049 - 8057 (2007/10/03)
Intramolecular element effects kBr/kCl for substitution of geminal bromochloroalkenes BrC(Cl)=C-(Br)Cl (1), BrC(Cl)=CCl2 (2), Me2C=C(Br)Cl (3), and XCH=C(Br)Cl (X = Cl, 4; X = Br, 5), with MeO- and RS- nucleophiles were investigated. 3 did not give substitution, and 4 and 5 gave substitution with MeO- via an initial elimination (to acetylene)-addition route, followed by further reactions. In reactions of 4 with thiolates, geminal element effects of 2-10 were obtained. Formation of RSC(Cl)=C(Cl)Y, Y = SR, Br, is ascribed to an initial halophilic reaction, followed by addition of RSCl to the formed acetylene. Reaction of 2 with MeO- gave a high vicinal element effect, and RS- gave a high geminal element effect. Reaction of 1 with both MeO- and RS- ions gave high (2 orders of magnitude) geminal element effects, which were interpreted as indicating a rate-determining C-X bond cleavage. This is supported by the high kBr/kCl intermolecular element effects (k(1)/k(Cl2C=CCl2) with MeO- and PhCH2S- ions. Mechanistic alternatives based on these observations are discussed.
