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2180-01-0

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2180-01-0 Usage

General Description

Selenium dicyanide, also known as selenium cyanide, is a chemical compound with the formula Se(CN)2. It is a toxic and highly reactive substance that is primarily used in research and laboratory settings. Selenium dicyanide is a colorless, crystalline solid that is soluble in water and other polar solvents. It is known to be unstable and can decompose into toxic hydrogen cyanide gas when heated or exposed to acids. Selenium dicyanide is not widely used in industrial applications due to its hazardous nature, but it is of interest in the scientific community for its potential use in chemical synthesis and as a reagent in certain types of chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 2180-01-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,8 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2180-01:
(6*2)+(5*1)+(4*8)+(3*0)+(2*0)+(1*1)=50
50 % 10 = 0
So 2180-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C2N2Se/c3-1-5-2-4

2180-01-0SDS

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 cyano selenocyanate

1.2 Other means of identification

Product number -
Other names Selenium cyanide

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:2180-01-0 SDS

2180-01-0Relevant articles and documents

13C NMR and FT-IR spectra of thiocyanogen, S2(CN)2, selenocyanogen, Se2(CN)2, and related compounds

Cataldo

, p. 681 - 688 (2000)

The pseudohalogens thiocyanogen [(SCN)2], sulfur dicyanide [S(CN)2], selenocyanogen [(SeCN)2], selenium dicyanide [Se(CN)2] and selenium diselenocyanate [Se(SeCN)2] have been prepared and studied by 13C NMR spectroscopy for the first time. The 13C NMR results confirm the structure previously assigned to these compounds on the basis of vibrational spectroscopy. Thiocyanogen, sulfur dicyanide, selenocyanogen and selenium dicyanide have been also studied as liquid film on KBr plate in the solid state (KBr pellet) by FT-IR spectroscopy and the data collected have been compared and discussed with previous results recorded on solutions in organic solvents. Good agreement with early results has been obtained. It has been confirmed by solid state 13C NMR-MAS that under mild conditions selenocyanogen disproportionates into selenium dicyanide and selenium diselenocyanate. By heating selenocyanogen above 180°C it polymerizes irreversibly into a brown polymer known as paraselenocyanogen whose FT-IR spectrum is surprisingly very similar to that of parathiocyanogen or polythiocyanogen, the product of self-polymerization of thiocyanogen. (C) 2000 Elsevier Science Ltd.

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