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58793-92-3

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58793-92-3 Usage

Explanation

The compound is composed of 9 carbon atoms, 14 hydrogen atoms, and 4 nitrogen atoms.

Explanation

It is a cationic compound with a triaza diene structure, which is a six-membered ring containing three nitrogen atoms.

Explanation

The triaza diene cation has a 6-cyanohexyl group attached to it, which is a hexyl chain with a cyano group (CN) at the sixth carbon.

Explanation

The compound can be used as a starting material for the synthesis of various organic molecules due to its versatile structure.

Explanation

1-(6-cyanohexyl)triaza-1,2-dien-2-ium can act as a ligand, coordinating with metal ions in catalytic processes, which can be useful in various chemical reactions.

Explanation

Due to its unique structure and properties, the compound has the potential to be utilized in a wide range of research and industrial processes, including the development of new materials, pharmaceuticals, and catalysts.

Type of compound

Triaza diene cation

Substituent

6-cyanohexyl

Applications

Organic chemistry building block

Use as a ligand

Coordination with metal ions

Versatility

Potential applications in research and industry

Check Digit Verification of cas no

The CAS Registry Mumber 58793-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,9 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58793-92:
(7*5)+(6*8)+(5*7)+(4*9)+(3*3)+(2*9)+(1*2)=183
183 % 10 = 3
So 58793-92-3 is a valid CAS Registry Number.

58793-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-azidoheptanenitrile

1.2 Other means of identification

Product number -
Other names 6-Cyan-hexylazid

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:58793-92-3 SDS

58793-92-3Upstream product

58793-92-3Relevant articles and documents

Poly(diiododiacetylene): Preparation, isolation, and full characterization of a very simple poly(diacetylene)

Luo, Liang,Wilhelm, Christopher,Sun, Aiwu,Grey, Clare P.,Lauher, Joseph W.,Goroff, Nancy S.

, p. 7702 - 7709 (2008/12/22)

Poly(diiodiacetylene), or PIDA, is a conjugated polymer containing the poly(diacetylene) (PDA) backbone but with only iodine atom substituents. The monomer diiodobutadiyne (1) can be aligned in the solid state with bis(nitrile) oxalamide hosts by hydrogen bonds between oxalamide groups and weak Lewis acid-base interactions (halogen bonds) between nitriles and iodoalkynes. The resulting cocrystals start out pale blue but turn shiny and copper-colored as the polymerization progresses. The development of a crystallization methodology that greatly improves the yield of PIDA to about 50% now allows the full characterization of the polymer by X-ray diffraction, solid-state 13C MAS NMR, Raman, and electron absorption spectroscopy. Comparison of a series of hosts reveals an odd-even effect in the topochemical polymerization, based on the alkyl chain length of the host. In the cocrystals formed with bis(pentanenitrile) oxalamide (4) and bis(heptanenitrile) oxalamide (6), the host/guest ratio is 1:2 and the monomer polymerizes spontaneously at room temperature, while in the case of bis(butanenitrile) oxalamide (3) and bis(hexanenitrile) oxalamide (5), where the host and guest form cocrystals in a 1:1 ratio, the polymerization is disfavored and does not go to completion. The topochemical polymerization can also be observed in water suspensions of micrometer-sized 6.1 cocrystals; the size distribution of these microcrystals, and the resulting polymer chains, can be controlled by sonication. Completely polymerized PIDA cocrystals show a highly resolved vibronic progression in their UV/vis absorption spectra. Extensive rinsing of the crystals in organic solvents such as methanol, THF, and chloroform separates the polymer from the soluble host. Once isolated, PIDA forms blue suspensions in a variety of solvents. The UV/vis absorption spectra of these suspensions match the cocrystal spectrum, without the vibronic resolution. However, they also include a new longer-wavelength absorption peak, associated with aggregation of the polymer chains.

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