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(diphenylcarbamimidoyl)selanyl is a chemical compound characterized by a selenium atom bonded to two phenyl groups and a carbamimidoyl group. It is recognized for its potential in organic synthesis and has garnered interest due to its possible biological and pharmaceutical applications.

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  • 16519-43-0 Structure
  • Basic information

    1. Product Name: (diphenylcarbamimidoyl)selanyl
    2. Synonyms:
    3. CAS NO:16519-43-0
    4. Molecular Formula: C13H12N2Se
    5. Molecular Weight: 274.1998
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16519-43-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (diphenylcarbamimidoyl)selanyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: (diphenylcarbamimidoyl)selanyl(16519-43-0)
    11. EPA Substance Registry System: (diphenylcarbamimidoyl)selanyl(16519-43-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 16519-43-0(Hazardous Substances Data)

16519-43-0 Usage

Uses

Used in Organic Synthesis:
(diphenylcarbamimidoyl)selanyl is utilized as a key intermediate in the synthesis of various organic compounds, contributing to the development of novel chemical entities.
Used in Antioxidant Applications:
In the pharmaceutical industry, (diphenylcarbamimidoyl)selanyl is used as an antioxidant agent for its ability to combat oxidative stress, which is a significant factor in the development of various diseases.
Used in Anti-inflammatory Applications:
(diphenylcarbamimidoyl)selanyl is employed as an anti-inflammatory agent, potentially mitigating the harmful effects of inflammation on the body and providing relief in conditions characterized by excessive inflammation.
Used in Antitumor Applications:
Within the realm of oncology, (diphenylcarbamimidoyl)selanyl is investigated as a potential antitumor agent, with its properties being studied for their impact on tumor growth and progression.
Used in Redox Signaling:
(diphenylcarbamimidoyl)selanyl is also used in the study of redox signaling, where it may play a role in modulating cellular processes and maintaining cellular homeostasis.
Used in Cellular Process Modulation:
(diphenylcarbamimidoyl)selanyl is further explored for its capacity to modulate cellular processes, which could have implications for understanding and treating various diseases at the cellular level.

Check Digit Verification of cas no

The CAS Registry Mumber 16519-43-0 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, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16519-43:
(7*1)+(6*6)+(5*5)+(4*1)+(3*9)+(2*4)+(1*3)=110
110 % 10 = 0
So 16519-43-0 is a valid CAS Registry Number.

16519-43-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-λ<sup>1</sup>-selanyl-N,N'-diphenylmethanimidamide

1.2 Other means of identification

Product number -
Other names N.N'-Diphenyl-selenharnstoff

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:16519-43-0 SDS

16519-43-0Relevant articles and documents

Efficient synthesis of selenoureas from the corresponding carbodiimides

Koketsu, Mamoru,Takakura, Naotaka,Ishihara, Hideharu

, p. 3075 - 3079 (2002)

Selenoureas were synthesized by the reaction of carbodiimides with LiA1HSeH in the presence of hydrogen chloride.

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.

Selenoureas for anion binding as molecular logic gates

Casula, Arianna,Begines, Paloma,Bettoschi, Alexandre,Fernandez-Bola?os, Josè G.,Isaia, Francesco,Lippolis, Vito,López, óscar,Picci, Giacomo,Andrea Scorciapino,Caltagirone, Claudia

supporting information, p. 11869 - 11872 (2017/11/06)

The first example of a molecular logic gate based on selenourea/anion host-guest interaction that performs a ternary logic operation using an 1H-NMR easy to read response output is described here. Selenoureas are very versatile receptors for anion binding, capable of forming both mono- and bi-coordinated adducts at room temperature in solution.

Polyfused nitrogen-containing heterocycles 23.* Methyl 4-hydroxy-3-phenyl-5-phenyl(alkyl)-2-phenyliminoselenazolidine-4-carboxylates and selenazolo[3,4-a]quinoxalin-4(5H)-one derivatives on their basis

Mamedov,Zhukova,Gubaidullin,Beschastnova,I. Kh. Rizvanov,Ya. A. Levin,Litvinov

experimental part, p. 1294 - 1302 (2010/10/04)

Condensation of methyl phenyl(alkyl)halopyrotartrates with N, N'-diphenylselenourea leads to the formation of methyl 4-hydroxy-3-phenyl-5- phenyl(alkyl)-2-phenyliminoselenazolidine-4-carboxylates, which undergo reaction with 1,2-phenylenediamines to give selenazolo-[3,4-a]quinoxalin-4(5H)-ones. ; 2009 Springer Science+Business Media, Inc.

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