15075-90-8 Usage
Uses
Used in Chemical Industry:
1,2-Dichloroethene-D2 is used as a solvent and in the manufacture of other chemicals for its ability to dissolve a wide range of substances and facilitate chemical reactions.
Used in Plastics Production:
1,2-Dichloroethene-D2 is used in the production of plastics due to its properties that contribute to the formation of desired plastic characteristics.
Used in Adhesives Production:
1,2-Dichloroethene-D2 is used in the production of adhesives, where its solvent properties help in creating effective bonding agents.
Used in Aerosol Formulations:
1,2-Dichloroethene-D2 is used as a solvent for aerosol formulations, providing a medium for the dispersion of active ingredients in spray products.
Used in Rubber Production:
1,2-Dichloroethene-D2 is utilized in the production of rubber, where it aids in the process of creating flexible and durable rubber materials.
Health and Safety Note:
1,2-Dichloroethene-D2 is classified as a hazardous substance. Exposure to high levels of 1,2-Dichloroethene-D2 can cause irritation to the skin, eyes, and respiratory system, necessitating proper handling and safety measures during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 15075-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,7 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15075-90:
(7*1)+(6*5)+(5*0)+(4*7)+(3*5)+(2*9)+(1*0)=98
98 % 10 = 8
So 15075-90-8 is a valid CAS Registry Number.
15075-90-8Relevant academic research and scientific papers
Preparation, Structure, and Nuclear Magnetic Resonance Properties of the Nine-vertex nido-Rhenaborane and Some Related Chemistry
Beckett, Michael A.,Bown, Mark,Fontaine, Xavier L. R.,Greenwood, Norman N.,Kennedy, John D.,Thornton-Pett, Mark
, p. 1969 - 1982 (2007/10/02)
Thermolysis of (1) in C2D2Cl4 solution gives the new, pale yellow air-stable compound (2) in 80 percent yield.Crystals of the CH2Cl2 hemisolvate of (2) are monoclinic, space group P21/c, with a = 1130.0(3), b = 1292.2(3), c = 2424.0(5) pm, β = 94.15(2) degree, and Z = 4; the molecular structure was refined to R = 0.0399, R' = 0.0454.The detailed n.m.r. behaviour of compound (2) together with data for previously reported rhodium and iridium analogues permits the location of the substituent site on previously unconfirmed and thence provides information on mechanistic pathways for the formation of these and related metallaboranes.Detailed n.m.r. data for the non-metalla analogues - and previously unassigned - provide information on their mechanism of formation and a comparison with the metallaborane analogues.The n.m.r. work includes extensive use of - COSY and - COSY experiments and establishes general points.
