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20395-25-9

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20395-25-9 Usage

Uses

1,1,3-Trichloropropane is a disinfection byproducts in chlorinated drinking water. Also, it is derived from Acrolein (A191200), which is used in the synthesis of acrylic acid.

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

20395-25-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,3-trichloropropane

1.2 Other means of identification

Product number -
Other names 1.1.3-Trichlorpropan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20395-25-9 SDS

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.

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