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1,3-Diiminobenz[f]isoindoline is a chemical compound belonging to the 1,3-diiminobenzisoindoline family, which is a type of aromatic amine. It has the chemical formula C14H8N4 and features a complex structure with multiple interconnected rings of atoms. Due to its limited study, there is scarce information available on its properties and applications. It is recommended to handle this chemical with caution, as the potential effects on human health and the environment are not well understood.

65558-69-2

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65558-69-2 Usage

Uses

Since the provided materials do not specify any particular applications for 1,3-diiminobenz[f]isoindoline, it is not possible to list its uses as per the given instructions. However, it is important to note that the compound's potential uses may be discovered in the future as more research is conducted on its properties and behavior.

Check Digit Verification of cas no

The CAS Registry Mumber 65558-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,5 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65558-69:
(7*6)+(6*5)+(5*5)+(4*5)+(3*8)+(2*6)+(1*9)=162
162 % 10 = 2
So 65558-69-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H9N3/c13-11-9-5-7-3-1-2-4-8(7)6-10(9)12(14)15-11/h1-6H,(H3,13,14,15)

65558-69-2SDS

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 1,3-Diiminobenz[<i>f</i>]isoindoline

1.2 Other means of identification

Product number -
Other names 3-iminobenzo[f]isoindol-1-amine

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:65558-69-2 SDS

65558-69-2Upstream product

65558-69-2Downstream Products

65558-69-2Relevant academic research and scientific papers

Optical recording medium

-

, (2008/06/13)

The present invention relates to an optical recording medium laminated having on a substrate a recording layer comprising an organic thin film containing a silicon naphthalocyanine compound represented by the following general formula (I): wherein L and L' each represents a group capable of linking to silicon.

SILICON PHTHALOCYANINE AND A SILICON NAPHTHALOCYANINE: SYNTHESIS, ELECTROCHEMISTRY, AND ELECTROGENERATED CHEMILUMINESCENCE.

Wheeler,Nagasubramanian,Bard,Schechtman,Dininny,Kenney

, p. 7404 - 7410 (2007/10/02)

The synthesis, spectral characterization, and electrochemical behavior of bis(tri-n-hexylsiloxy)(2,3-phthalocyaninato)silicon left bracket SiPc(OR)//2 right bracket , its dimer left bracket RO(SiPcO)//2R right bracket , and its naphthalocyanine analog left bracket SiNc(OR)//2 right bracket are described. All compounds show near-UV absorption corresponding to Soret and N bands and intense absorption in the visible - near-IR region corresponding to Q bands. In CH//2Cl//2, within the solvent stability limit, there are two reductions and one oxidation for SiPc(OR)//2 and two reductions and two oxidations for RO(SiPcO)//2R and SiNc(OR)//2; all appear as reversible one-electron waves, although n equals 2 for the dimer. The difference in the peak potentials of the first oxidation and first reduction waves agrees well with the excitation energy and fluorescence (corresponding to Q bands) of SiPc(OR)//2 and SiNc(OR)//2.

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