872-17-3 Usage
Description
11-Chloro-1-undecane is an organic compound with the chemical formula C11H21Cl. It is a colorless liquid with a chloroalkane structure, featuring a chlorine atom attached to an 11-carbon chain. 11-CHLORO-1-UNDECENE is known for its reactivity and is commonly used as an intermediate in the synthesis of various chemicals.
Uses
Used in Polymer Industry:
11-Chloro-1-undecane is used as a comonomer in copolymerizations of propylene. Its incorporation into the polymer chain enhances the properties of the resulting copolymer, such as its flexibility, toughness, and chemical resistance.
Used in Chemical Synthesis:
11-Chloro-1-undecane is used in the preparation of unsaturated fatty acids, which are essential components in the production of various industrial products, such as lubricants, surfactants, and plasticizers. These unsaturated fatty acids also serve as important intermediates in the synthesis of other valuable chemicals.
Used in Terpolymerization Process:
In the terpolymerization process, 11-chloro-1-undecane is used as a comonomer along with ethylene and propylene. This process is catalyzed by a metallocene catalyst, such as bis(cyclopentadienyl)methyl aluminum oxide (Me2Al(OC5H4)2). The resulting terpolymers exhibit improved mechanical properties and chemical resistance, making them suitable for various applications in the plastics and rubber industries.
Overall, 11-chloro-1-undecane plays a significant role in the chemical and polymer industries, contributing to the development of new materials with enhanced properties and performance.
Check Digit Verification of cas no
The CAS Registry Mumber 872-17-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 872-17:
(5*8)+(4*7)+(3*2)+(2*1)+(1*7)=83
83 % 10 = 3
So 872-17-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H21Cl/c1-2-3-4-5-6-7-8-9-10-11-12/h2H,1,3-11H2
872-17-3Relevant articles and documents
Copper-catalyzed trifluoromethylthiolation of primary and secondary alkylboronic acids
Shao, Xinxin,Liu, Tianfei,Lu, Long,Shen, Qilong
supporting information, p. 4738 - 4741 (2015/04/27)
A Cu-catalyzed trifluoromethylthiolation of primary and secondary alkylboronic acids with an electrophilic trifluoromethylthiolating reagent is described. Tolerance for a variety of functional groups was observed.
