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Trichloro-ethylol-urea, also known as 1,1,1-trichloro-2-(2-chloroethoxy)-2-(2-chloroethoxy)-2-urea, is a chemical compound with the molecular formula C5H8Cl6N2O2. It is a white crystalline solid that is soluble in water and has a molecular weight of 322.33 g/mol. Trichloro-ethylol-urea is primarily used as a herbicide, specifically for controlling broadleaf and grassy weeds in various crops. It works by inhibiting photosynthesis in plants, leading to their death. Due to its potential environmental and health risks, its use has been restricted or banned in some countries.

2000-40-0

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2000-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2000-40-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,0 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2000-40:
(6*2)+(5*0)+(4*0)+(3*0)+(2*4)+(1*0)=20
20 % 10 = 0
So 2000-40-0 is a valid CAS Registry Number.
InChI:InChI=1/C3H5Cl3N2O2/c4-3(5,6)1(9)8-2(7)10/h1,9H,(H3,7,8,10)

2000-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,2,2-trichloro-1-hydroxyethyl)urea

1.2 Other means of identification

Product number -
Other names Chloralurea

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:2000-40-0 SDS

2000-40-0Relevant academic research and scientific papers

A novel convenient synthesis of 5-acyl-1,2-dihydropyrimidin-2-ones via 4-trichloromethyl-1,2,3,4-tetrahydropyrimidin-2-ones

Fesenko, Anastasia A.,Solovyev, Pavel A.,Shutalev, Anatoly D.

scheme or table, p. 940 - 946 (2010/03/24)

A novel four-step methodology for the synthesis of 5-acyl-1,2-dihydropyrimidin-2-ones has been developed. The reaction of readily available N-[(1-acetoxy-2,2,2-trichloro)ethyl]ureas with Na-enolates of 1,3-diketones or β-oxoesters followed by heterocycliz

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