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26223-16-5

1,2,3-selenadiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 26223-16-5 Structure

  • Basic information

    1. Product Name: 1,2,3-selenadiazole
    2. Synonyms:
    3. CAS NO:26223-16-5
    4. Molecular Formula: C2H2N2Se
    5. Molecular Weight: 133.0107
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 26223-16-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 147.6°C at 760 mmHg
    3. Flash Point: 43°C
    4. Appearance: N/A
    5. Density: N/A
    6. Vapor Pressure: 5.57mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,2,3-selenadiazole(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,2,3-selenadiazole(26223-16-5)
    12. EPA Substance Registry System: 1,2,3-selenadiazole(26223-16-5)

  • 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: 26223-16-5(Hazardous Substances Data)

26223-16-5 Usage

Chemical structure

A heterocyclic organic compound containing a five-membered ring with three nitrogen atoms and one selenium atom.

Family

A member of the selenadiazole family.

Structural similarity

Similar to other nitrogen-containing heterocycles such as pyrazole and triazole.

Chemical and biological properties

Exhibits a range of interesting chemical and biological properties.

Field of interest

A topic of interest in medicinal chemistry and material science.

Potential applications

a. Building block in the synthesis of novel pharmaceuticals.
b. Ligand in coordination chemistry.

Potential applications

Has potential applications in various fields, including pharmaceuticals and materials science.

Investigated properties

a. Antioxidant properties.
b. Anti-cancer properties.

Versatility

A versatile compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 26223-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,2 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26223-16:
(7*2)+(6*6)+(5*2)+(4*2)+(3*3)+(2*1)+(1*6)=85
85 % 10 = 5
So 26223-16-5 is a valid CAS Registry Number.

26223-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3-Selenadiazole

1.2 Other means of identification

Product number -
Other names -

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:26223-16-5 SDS

26223-16-5Upstream product

26223-16-5Relevant articles and documents

2-METHYLENE-1,3-DISELENOLE:A PRECURSOR OF TETRASELENAFULVALENE (TSeF)

Jackson, Yvette A.,White, Christy L.,Lakshmikantham, M. V.,Cava, Michael P.

, p. 5635 - 5636 (1987)

The preparation of methylene-1,3-diselenole and its ready conversion to TSeF are discussed.

α,β-Unsaturated Thiolates and Their Analogs in Cycloaddition Reactions. XXIII. A Convenient One-Pot Synthesis of 2-Phenylimino-1,3-thiaselenoles and -1,3-diselenoles

Zmitrovich,Petrov

, p. 1812 - 1816 (2007/10/03)

2-Phenylimino-1,3-diselenole, 2-phenylimino-1,3-thiaselenole, and 4-methyl-2-phenylimino-1,3-diselenole were synthesized for the first time by successive reactions of 1,2,3-thia(selena)diazoles with potassium tert-butoxide and phenyl isoselenocyanate with

Synthesis of sym-(E/Z)-Diselenadithiafulvalene

Lakshmikantham, M.V.,Cava, Michael P.

, p. 2632 - 2636 (2007/10/02)

sym-Diselenadithiafulvalene (3) has been synthesized as an inseparable E,Z isomer mixture by two fundamentally different routes.The first synthesis proceeds via ethylene diselenocyanate (9), ethane-1,2-diselenol (8), 1,3-Diselenolane-2-thione (7), 4,5-bis(carbomethoxy)-1,3-thiaselenole-2-selone (12),and tetrakis(carbomethoxy)-sym-diselenadithiafulvalene (13).The second synthesis,which involves a greatly improved route to 1,3-thiaselenole-2-selone (18),provides the most practical method available for the preparation of larger quantities of 3.

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