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N,N-Dimethyl-N'-phenylselenourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21347-32-0

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21347-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21347-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,4 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21347-32:
(7*2)+(6*1)+(5*3)+(4*4)+(3*7)+(2*3)+(1*2)=80
80 % 10 = 0
So 21347-32-0 is a valid CAS Registry Number.

21347-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dimethyl-3-phenyl-selenourea

1.2 Other means of identification

Product number -
Other names N,N-Dimethyl-N'-phenylselenoharnstoff

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:21347-32-0 SDS

21347-32-0Relevant academic research and scientific papers

One-Pot Four-Component Assembling for Selenoureas

Li, Lai,Wu, Jiaqi,Wei, Linsha,Lu, Jianmei,Jiang, Xuefeng

, p. 446 - 454 (2020/12/23)

An efficient and practical method for the straightforward construction of unsymmetrical selenoureas and cycloselenoureas via the combination of selenium powder, chloroform, and two different amines was comprehensively achieved in one-pot with only the assistance of a base under mild conditions. Thirty-three new structures of unsymmetrical selenoureas including three chiral examples and eight cycloselenoureas were achieved. 1,1-Dimethyl-3-phenylselenourea II, which shows good fungicidal activity, was practically synthesized through this protocol in gram-scale. Isoselenocyanate was further confirmed as a key intermediate by control experiment.

Synthesis and pesticidal properties of thio and seleno analogs of some common urea herbicides

Zakrzewski, Jerzy,Krawczyk, Maria

experimental part, p. 1880 - 1903 (2010/02/28)

Thio and seleno analogs of fenuron, isoproturon, chlorotoluron, metoxuron, monuron, and diuron were synthesized from the corresponding aryl amines. Their reaction with thiophosgene leads to isothiocyanates. Aryl amines were also converted (via isocyanides) to isoselenocyanates. The reaction of both isothio- and isoselenocyanates with dimethylamine affords the corresponding thio and seleno analogs of the above-mentioned urea herbicides. Herbicidal activity of the synthesized compounds was slightly lower than the activity of the parent urea herbicides. The thio and seleno analogs as well as the parent ureas showed good fungicidal activity at a concentration of 200 ppm against selected fungi.

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