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1,4-Cyclohexadiene-1,4-diamine, 3,6-diimino- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24196-90-5

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24196-90-5 Usage

Diamine

Contains two amino groups

Explanation

A diamine is a compound with two amine groups (-NH2) attached to the molecule. These groups are important for the compound's reactivity and potential applications.

Explanation

The compound has a ring structure with six atoms, which is common in organic chemistry and can influence the compound's properties and reactivity.

Explanation

Due to its structure and functional groups, 1,4-Cyclohexadiene-1,4-diamine, 3,6-diiminocan be used as a starting material or intermediate in the synthesis of various organic compounds.

Explanation

The presence of multiple nitrogen atoms and a cyclic structure can make 1,4-Cyclohexadiene-1,4-diamine, 3,6-diimino- reactive, which may lead to hazardous situations if not handled properly.

Explanation

Due to its reactivity and the presence of nitrogen atoms, 1,4-Cyclohexadiene-1,4-diamine, 3,6-diimino- may pose risks to human health and the environment if not handled with care. Proper safety measures and precautions should be taken when working with 1,4-Cyclohexadiene-1,4-diamine, 3,6-diimino-.

Explanation

The appearance of the compound (e.g., color, state of matter) is not mentioned in the given information. This can vary depending on the specific conditions and purity of the sample.

Cyclic compound

Six-membered ring

Potential uses

Organic synthesis and building block for other organic compounds

Reactivity

Potentially reactive

Hazards

Potential hazards associated with handling

Appearance

Not specified in the provided material

Check Digit Verification of cas no

The CAS Registry Mumber 24196-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,9 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24196-90:
(7*2)+(6*4)+(5*1)+(4*9)+(3*6)+(2*9)+(1*0)=115
115 % 10 = 5
So 24196-90-5 is a valid CAS Registry Number.

24196-90-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-diimino-1,4-cyclohexadiene-1,4-diamine

1.2 Other means of identification

Product number -
Other names 2,5-Diamino-[1,4]benzochinon-diimin

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:24196-90-5 SDS

24196-90-5Relevant academic research and scientific papers

Extendable nickel complex tapes that reach NIR absorptions

Audi, Hassib,Chen, Zhongrui,Charaf-Eddin, Azzam,D'Alo, Anthony,Canard, Gabriel,Jacquemin, Denis,Siri, Olivier

, p. 15140 - 15143 (2014)

Stepwise synthesis of linear nickel complex oligomer tapes with no need for solid-phase support has been achieved. The control of the length in flat arrays allows a fine-tuning of the absorption properties from the UV to the NIR region.

Polybenzobisimidazole-derived two-dimensional supramolecular polymer

Seo, Wanji,Carpenter, Keith L.,Gaugler, James A.,Shao, Wenting,Werling, Keith A.,Fournier, Philip M.,Lambrecht, Daniel S.,Star, Alexander

, p. 1095 - 1101 (2017)

We report a novel crystalline supramolecular polybenzobisimidazole (SP-PBBI) capable of providing a two-dimensional polymer (2DSP-PBBI) by liquid-phase exfoliation. A regular arrangement of rigid rod-like polybenzobisimidazole (PBBI) chains is achieved by interchain hydrogen bonding. Titration of 2DSP-PBBI with cobalt chloride (CoCl2) using UV-Vis spectroscopy demonstrates the presence of bidentate NO ligands on the PBBI backbone and NO–Co(II) complexation. Imaging analysis using atomic force microscopy (AFM) reveals the planar surface morphology of exfoliated 2DSP-PBBI sheets with lateral dimensions of 1 μm and thickness of 30 nm. The size of the polymer crystal growth is tuned by employing condensation/precipitation polymerization under nonisothermal conditions.

UV-induced single and double hydrogen-atom migrations in 3,6-diimino-1,4-cyclohexadiene-1,4-diamine in a low-temperature argon matrix

Ujike, Kenji,Kudoh, Satoshi,Nakata, Munetaka

, p. 52 - 56 (2005)

Isomerization induced by ultraviolet radiation due to intramolecular hydrogen-atom migration in 3,6-diimino-1,4-cyclohexadiene-1,4-diamine (DCD) was studied by matrix-isolation Fourier transform infrared (IR) spectroscopy and density functional theory (DFT) calculation. Two isomers produced by single and double inversion of the hydrogen atom(s) around the CN bond(s) were identified using the wavelength dependence of the IR band-intensity changes. In addition, the IR bands of an intermediate produced by single hydrogen-atom transfer from the amino to the imino group (C-NH2?NHC) in the hydrogen bond were measured and identified by a comparison with the calculated spectral patterns. These observations confirm stepwise photoisomerization of DCD.

METHOD FOR PREPARING METAL-ORGANIC FRAMEWORK INCLUDING TWO ORGANIC LIGANDS

-

Paragraph 0118-0120, (2021/06/22)

Disclosed are a method for preparing a method for preparing a metal-organic framework comprising two organic ligands, and a metal-organic framework prepared by the preparation method. Since the metal-organic framework has high porosity and excellent electrical conductivity, when the metal-organic framework is used for electrodes such as supercapacitors or secondary batteries and the like, energy density and output characteristics of a device can be improved.

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