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10,10-diphenyl-5,10-dihydrodibenzo[b,e][1,4]azasiline is a complex organic compound with the molecular formula C24H21N. It is a derivative of dibenzo[b,e][1,4]azasiline, featuring two phenyl groups attached to the 10th carbon atom of the molecule. 10,10-diphenyl-5,10-dihydrodibenzo[b,e][1,4]azasiline is characterized by its unique structure, which includes a seven-membered ring with alternating nitrogen and carbon atoms, and a dihydrodibenzene moiety. It is synthesized through various chemical reactions and is used in the pharmaceutical industry as a building block for the development of potential therapeutic agents. Due to its specific structure, it may exhibit interesting chemical and biological properties, making it a subject of interest for researchers in the field of medicinal chemistry.

3508-62-1

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3508-62-1 Usage

Molecular structure

10,10-diphenyl-5,10-dihydrodibenzo[b,e][1,4]azasiline has a complex molecular structure consisting of two benzene rings connected by a five-membered nitrogen-containing ring.

Type of compound

It is a type of azasiline compound, which incorporates silicon and nitrogen atoms in its ring structure.

Potential applications

This chemical has potential applications in materials science, organic synthesis, and pharmaceutical research due to its unique structure and properties.

Safety precautions

As with any chemical compound, proper handling and safety precautions should be observed when working with 10,10-diphenyl-5,10-dihydrodibenzo[b,e][1,4]azasiline to minimize potential hazards.

Physical properties

The specific physical properties of 10,10-diphenyl-5,10-dihydrodibenzo[b,e][1,4]azasiline, such as melting point, boiling point, and solubility, are not provided in the material.

Chemical properties

The specific chemical properties of 10,10-diphenyl-5,10-dihydrodibenzo[b,e][1,4]azasiline, such as reactivity, stability, and chemical reactions, are not provided in the material.

Synthesis

The method of synthesis for 10,10-diphenyl-5,10-dihydrodibenzo[b,e][1,4]azasiline is not provided in the material.

Stability

The stability of 10,10-diphenyl-5,10-dihydrodibenzo[b,e][1,4]azasiline under various conditions, such as temperature, pressure, and exposure to light or air, is not provided in the material.

Hazards

The specific hazards associated with 10,10-diphenyl-5,10-dihydrodibenzo[b,e][1,4]azasiline, such as toxicity, flammability, and reactivity with other substances, are not provided in the material. However, it is mentioned that proper handling and safety precautions should be observed when working with this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 3508-62-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,0 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3508-62:
(6*3)+(5*5)+(4*0)+(3*8)+(2*6)+(1*2)=81
81 % 10 = 1
So 3508-62-1 is a valid CAS Registry Number.

3508-62-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 10,10-diphenyl-5,10-dihydro-phenazasiline

1.2 Other means of identification

Product number -
Other names 10,10-Diphenyl-5,10-dihydro-phenazasilin

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:3508-62-1 SDS

3508-62-1Downstream Products

3508-62-1Relevant academic research and scientific papers

Thermally Activated Delayed Fluorescence from Azasiline Based Intramolecular Charge-Transfer Emitter (DTPDDA) and a Highly Efficient Blue Light Emitting Diode

Sun, Jin Won,Baek, Jang Yeol,Kim, Kwon-Hyeon,Moon, Chang-Ki,Lee, Jeong-Hwan,Kwon, Soon-Ki,Kim, Yun-Hi,Kim, Jang-Joo

, p. 6675 - 6681 (2015)

For electroluminescence with delayed fluorescence, the azasiline unit has been introduced for the first time as a donor in a thermally activated delayed fluorescence (TADF) material. The TADF material (DTPDDA) shows strong intramolecular charge transfer (CT) character with large spatial separation with the acceptor of triazine leading to narrow splitting of singlet and triplet excited states for the efficient reverse intersystem crossing (RISC). A blue organic light emitting diode (OLED) based on DTPDDA not only displays deep blue in the Commission Internationale de L'Eclairage (CIE) coordinates of (0.149, 0.197) but also exhibits a high external quantum efficiency (EQE) of 22.3% which is the highest value ever reported for a blue fluorescent OLED. Theoretical prediction based on transient photoluminescence (PL) and optical simulation result agrees well with the achieved EQE indicating the successful conversion of triplet excitons to singlet in the blue fluorescent OLED by using DTPDDA.

Preparation method of 10,10 - diphenyl silicon heteroacridine

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, (2021/11/06)

The invention discloses a preparation method of 10,10 - diphenylsilicon heteroacridine, and belongs to the field of fine chemical engineering. The technical problem to be solved by the invention is that the implementation cost is low. The method has the a

ORGANIC ELECTROLUMINESCENCE DEVICE AND FUSED POLYCYCLIC COMPOUND FOR ORGANIC ELECTROLUMINESCENCE DEVICE

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, (2020/12/13)

An organic electroluminescence device of an embodiment includes oppositely disposed first electrode and second electrode, and a plurality of organic layers disposed between the first electrode and the second electrode, wherein at least one from among the organic layers includes a fused polycyclic compound represented by Formula 1 below, thereby showing improved emission efficiency.

Novel organic semiconductor compound and organic light emitting device using the same

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, (2016/10/10)

The present invention relates to a novel organic semiconductor compound, and an organic electroluminescent device using the same. More particularly, the organic semiconductor compound according to the present invention is an azasiline derivative with a rigid structure having an electron doner and an electron acceptor in the molecule, and can embody excellent oxidation stability and light emitting characteristics. The organic electroluminescent device using the same has a high purity blue color having high quantum efficiency. The organic semiconductor compound is represented by chemical formula 1.

ORGANIC ELECTROLUMINESCENCE ELEMENT AND MATERIAL FOR ORGANIC ELECTROLUMINESCENCE ELEMENT

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, (2017/04/12)

Provided are a novel organic electroluminescent device material and an organic electroluminescent device using the same. The organic electroluminescent device material includes a compound represented by the following formula (1). The organic electrolumine

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