1002-70-6 Usage
Uses
Used in Chemical Synthesis:
1-Decene, 10-chlorois used as an intermediate in the synthesis of various organic compounds, including surfactants, detergents, and other specialty chemicals. Its unique structure allows for versatile chemical reactions, making it a valuable component in the production of a wide range of products.
Used in Polymer and Plastic Production:
This chloro-substituted alkene is also utilized in the manufacturing of polymers and plastics. Its presence in the polymerization process can influence the properties of the resulting materials, such as flexibility, strength, and durability.
Used in Specialty Chemical Applications:
1-Decene, 10-chlorofinds use in certain specialty chemical applications where its specific chemical properties are required. These applications can include the production of pharmaceuticals, agrochemicals, or other high-value chemical products that benefit from its unique structure and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 1002-70-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1002-70:
(6*1)+(5*0)+(4*0)+(3*2)+(2*7)+(1*0)=26
26 % 10 = 6
So 1002-70-6 is a valid CAS Registry Number.
1002-70-6Relevant academic research and scientific papers
Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling
Longwitz, Lars,Jopp, Stefan,Werner, Thomas
, p. 7863 - 7870 (2019/06/27)
A catalytic system for the chlorination of alcohols under Appel conditions was developed. Benzotrichloride is used as a cheap and readily available chlorinating agent in combination with trioctylphosphane as the catalyst and phenylsilane as the terminal reductant. The reaction has several advantages over other variants of the Appel reaction, e.g., no additional solvent is required and the phosphane reagent is used only in catalytic amounts. In total, 27 different primary, secondary, and tertiary alkyl chlorides were synthesized in yields up to 95%. Under optimized conditions, it was also possible to convert epoxides and an oxetane to the dichlorinated products.
