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Selenourea, N-(4-methoxyphenyl)-N'-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16519-53-2

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16519-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16519-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,1 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16519-53:
(7*1)+(6*6)+(5*5)+(4*1)+(3*9)+(2*5)+(1*3)=112
112 % 10 = 2
So 16519-53-2 is a valid CAS Registry Number.

16519-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-methoxyphenyl)-N'-phenylselenourea

1.2 Other means of identification

Product number -
Other names 1-(4-Methoxy-phenyl)-3-phenyl-selenourea

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:16519-53-2 SDS

16519-53-2Relevant 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.

Tunable NIR-II emitting silver chalcogenide quantum dots using thio/selenourea precursors: Preparation of an MRI/NIR-II multimodal imaging agent

Basel, Siddhant,Bhardwaj, Karishma,Borthakur, Sukanya,Brito, Beatriz,Clarke, Mitchell,Pariyar, Anand,Pradhan, Sajan,Roy, Pankaj,Saikia, Lakshi,Shankar, Amit,Stasiuk, Graeme J.,Tamang, Sudarsan,Thapa, Surakcha

supporting information, p. 15425 - 15432 (2020/11/18)

Aqueous-stable, Cd- and Pb-free colloidal quantum dots with fluorescence properties in the second near-infrared region (NIR-II, 1000-1400) are highly desirable for non-invasive deep-tissue optical imaging and biosensing. The low band-gap semiconductor, silver chalcogenide, offers a non-toxic and stable alternative to existing Pd, As, Hg and Cd-based NIR-II colloidal quantum dots (QDs). We report facile access to NIR-II emission windows with Ag2X (X = S, Se) QDs using easy-to-prepare thio/selenourea precursors and their analogues. The aqueous phase transfer of these QDs with a high conservation of fluorescence quantum yield (retention up to ~90%) and colloidal stability is demonstrated. A bimodal NIR-II/MRI contrast agent with a tunable fluorescence and high T1 relaxivity of 408 mM-1 s-1 per QD (size ~ 2.2 nm) and 990 mM-1 s-1 per QD (size ~ 4.2 nm) has been prepared by grafting 50 and 120 monoaqua Gd(iii) complexes respectively to two differently sized Ag2S QDs. The size of the nanocrystals is crucial for tuning the Gd payload and the relaxivity.

Synthesis method of selenourea derivative

-

Paragraph 0097-0114, (2020/04/22)

The invention discloses a synthesis method of a selenourea derivative, and the method comprises the following steps: mixing 1-5 parts by mole of a first amine, 5-12 parts by mole of chloroform, 2-8 parts by mole of an alkaline substance and a reaction solvent under the protection of nitrogen or argon, and reacting for 1-6 hours while stirring at 25-80 DEG C; adding 1-6 parts of selenium powder, 1-4 parts of an alkaline substance, 1 part of morpholine or 1 part of a second amine, carrying out a stirring reaction at 25-80 DEG C for 3-8h to obtain a reaction solution, and carrying out post-treatment on the reaction solution to obtain the selenourea derivative, the synthesis method of the selenourea derivative disclosed by the invention has the beneficial effects that (1) the raw materials aresimple and easy to obtain, and the reaction conditions are mild; (2) the product yield is relatively ideal; and (3) the synthesis of the asymmetric selenourea derivative can be realized.

Synthesis of 4-(phenylamino)quinazoline-2(1H)-selones and diselenides from isoselenocyanates: Dimroth rearrangement of an intermediate

Atanassov, Plamen K.,Linden, Anthony,Heimgartner, Heinz

, p. 1873 - 1887 (2007/10/03)

The reaction of anthranilonitriles 8 with phenyl isoselenocyanates (1a) in dry pyridine under reflux gave 4-(phenylamino)quinazoline-2(1H)-selones 9 (Scheme 2). They are easily oxidized and converted to diselenides of type 11. The analogous reaction of 8a

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