20395-25-9 Usage
Description
1,1,3-Trichloropropane is an organic compound with the chemical formula C3H5Cl3. It is a colorless liquid with a chloroform-like odor and is known for its use as a solvent and in the production of various chemicals.
Uses
1. Used in Chlorinated Drinking Water:
1,1,3-Trichloropropane is used as a disinfection byproduct in chlorinated drinking water. It is formed during the process of water treatment, where chlorine is used to kill bacteria and other microorganisms. However, the formation of 1,1,3-trichloropropane and other byproducts is a concern due to their potential health effects.
2. Used in Chemical Synthesis:
1,1,3-Trichloropropane is derived from Acrolein (A191200), which is used in the synthesis of acrylic acid. Acrylic acid is an important industrial chemical used in the production of various products, including plastics, coatings, and textiles. The use of 1,1,3-trichloropropane in this process highlights its role as an intermediate in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 20395-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,9 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20395-25:
(7*2)+(6*0)+(5*3)+(4*9)+(3*5)+(2*2)+(1*5)=89
89 % 10 = 9
So 20395-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H5Cl3/c4-2-1-3(5)6/h3H,1-2H2
20395-25-9Relevant articles and documents
Hydrodehalogenation of alkyl halides catalyzed by a trichloroniobium complex with a redox active α-diimine ligand
Nishiyama, Haruka,Hosoya, Hiromu,Parker, Bernard F.,Arnold, John,Tsurugi, Hayato,Mashima, Kazushi
supporting information, p. 7247 - 7250 (2019/07/02)
A high-valent d0 niobium(v) complex, (α-diimine)NbCl3 (1), bearing a dianionic redox-active α-diimine ligand served as a catalyst for a hydrodehalogenation reaction of alkyl halides in the presence of PhSiH3. During the catalytic reaction, the redox-active α-diimine ligand allowed the complex to reversibly release and accept one-electron through switching its coordination mode between a dianionic folded form and a monoanionic planar one.
