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9,10-Bis(4-formylphenyl)anthracene is a chemical compound with the molecular formula C30H20O2. It is a derivative of anthracene, featuring a central anthracene backbone with two formylphenyl groups attached at the 9 and 10 positions. 9,10-Bis(4-formylphenyl)anthracene is known for its photophysical properties and potential applications in various fields.

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  • 324750-99-4 Structure
  • Basic information

    1. Product Name: 9,10-Bis(4-formylphenyl)anthracene
    2. Synonyms: 9,10-Bis(4-formylphenyl)anthracene
    3. CAS NO:324750-99-4
    4. Molecular Formula: C28H18O2
    5. Molecular Weight: 386.44
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 324750-99-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 9,10-Bis(4-formylphenyl)anthracene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9,10-Bis(4-formylphenyl)anthracene(324750-99-4)
    11. EPA Substance Registry System: 9,10-Bis(4-formylphenyl)anthracene(324750-99-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 324750-99-4(Hazardous Substances Data)

324750-99-4 Usage

Uses

Used in Organic Synthesis:
9,10-Bis(4-formylphenyl)anthracene is used as a building block in organic synthesis for the development of new organic materials and fluorescent compounds. Its unique structure and properties make it a valuable component in creating advanced materials with specific characteristics.
Used in Materials Science:
In the field of materials science, 9,10-Bis(4-formylphenyl)anthracene is utilized for its potential in creating innovative materials with applications in various industries. Its ability to form new compounds and structures contributes to the advancement of material technologies.
Used in Optoelectronic Devices:
9,10-Bis(4-formylphenyl)anthracene is used as a component in optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics. Its photophysical properties make it suitable for these applications, where light emission and energy conversion are crucial.
Used in Photodynamic Therapy for Cancer Treatment:
In the medical field, specifically in cancer treatment, 9,10-Bis(4-formylphenyl)anthracene has been investigated for its potential use in generating singlet oxygen in photodynamic therapy. This application takes advantage of its ability to produce reactive oxygen species, which can be effective in destroying cancer cells.
Overall, 9,10-Bis(4-formylphenyl)anthracene is a versatile chemical compound with a wide range of applications across different industries, from organic synthesis and materials science to optoelectronics and medical treatments. Its unique properties and potential uses make it an important compound for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 324750-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,4,7,5 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 324750-99:
(8*3)+(7*2)+(6*4)+(5*7)+(4*5)+(3*0)+(2*9)+(1*9)=144
144 % 10 = 4
So 324750-99-4 is a valid CAS Registry Number.

324750-99-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[10-(4-formylphenyl)anthracen-9-yl]benzaldehyde

1.2 Other means of identification

Product number -
Other names 9,10-BIS(4-FORMYLPHENYL)ANTHRACENE

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:324750-99-4 SDS

324750-99-4Relevant articles and documents

Luminescence Ratiometric Nanothermometry Regulated by Tailoring Annihilators of Triplet–Triplet Annihilation Upconversion Nanomicelles

Chen, Shuoran,Li, Lin,Song, Yanlin,Wang, Xiaomei,Xu, Lei,Ye, Changqing,Zhang, Chun

supporting information, p. 26725 - 26733 (2021/11/23)

Triplet–triplet annihilation (TTA) upconversion is a special non-linear photophysical process that converts low-energy photons into high-energy photons based on sensitizer/annihilator pairs. Here, we constructed a novel luminescence ratiometric nanothermo

Mechanochemical generation of singlet oxygen

Akkaya, Engin U.,Aydonat, Simay,Baytekin, Bilge,Beduk, Tutku,Canyurt, Merve,Turksoy, Abdurrahman,Yildiz, Deniz

, p. 9182 - 9186 (2020/03/19)

Controlled generation of singlet oxygen is very important due to its involvement in scheduled cellular maintenance processes and therapeutic potential. As a consequence, precise manipulation of singlet oxygen release rates under mild conditions, is crucia

Efficient synthesis of organic semiconductors by Suzuki-Miyaura coupling in an aromatic micellar medium

Sanzone, Alessandro,Mattiello, Sara,Garavaglia, Giulia Maria,Calascibetta, Adiel Mauro,Ceriani, Chiara,Sassi, Mauro,Beverina, Luca

supporting information, p. 4400 - 4405 (2019/08/21)

Micellar catalysis enables carrying out Suzuki-Miyaura couplings in water under exceptionally mild conditions. Extension of such a protocol to the sustainable synthesis of highly conjugated, poorly soluble materials like [1]benzothieno[3,2-b][1]benzothiop

Anthracene derivatives having broad-spectrum up-conversion white-light emission characteristic and weak-light up-conversion white light system

-

Paragraph 0023, (2019/10/01)

The invention discloses anthracene derivatives having a broad-spectrum up-conversion white-light emission characteristic and a weak-light up-conversion white light system. The derivatives having the broad-spectrum up-conversion white-light emission charac

Organic light-emitting material with anthracene structure and organic light-emitting device with anthracene structure

-

, (2018/07/30)

The invention provides an organic light-emitting material with anthracene structure and an organic light-emitting device with anthracene structure and belongs to the technical field of organic photoelectric materials. The organic light-emitting material with anthracene structure comprises anthracene rings that are a blue light-emitting material parent nucleus structure having excellent performanceand having high triplet state energy level and wide energy gap; by connecting benzimidazole groups to molecules, the material is provided with improved electron transport capacity so that carrier transport is balanced. Compared with the prior art, the organic light-emitting material with anthracene structure applied to organic light-emitting devices, particularly as blue objective material in a light-emitting layer has higher luminous efficiency.

Reaction type luminous agent 9, 10 - diphenyl anthracene derivative and its preparation method and by the preparation of high-efficient light conversion system

-

Paragraph 0035-0038, (2019/01/08)

The invention discloses reaction type luminous agent 9, 10 - diphenyl anthracene derivative and its preparation method and by the preparation of high-efficient light conversion system, through the anthracycline 9, 10 - bits into the active group (alcohol

The relationship between molecular structure and electronic properties in dicyanovinyl substituted acceptor-donor-acceptor chromophores

Tarku?, Simge,Eelkema, Rienk,Grozema, Ferdinand C.

supporting information, p. 4994 - 5004 (2017/07/27)

In this contribution we describe a combined experimental and theoretical study of the relation between the molecular structure and the electronic properties of conjugated donor-acceptor type chromophores for light-harvesting applications. A series of model systems was synthesized where a central anthracene (electron donor) is connected to dicyanovinyl units (electron acceptor) through a π-conjugated spacer. The study of the redox and optical properties of these chromophores and of reference compounds without dicyanovinyl units allows us correlate the electronic properties to the presence of the electron withdrawing groups and the molecular conformation. Comparison with calculated electronic structure shows that the construction of chromophores that consist of electron donating and accepting units does not always follow the simple rules that are generally used in the design of such molecules. The results show a subtle relation between the charge transfer character and the geometry of the molecules. In some cases this leads to significant contribution of charge transfer excitation to the absorption spectra of some chromophores while such contributions are completely absent in others.

Suzuki-Miyaura Micellar Cross-Coupling in Water, at Room Temperature, and under Aerobic Atmosphere

Mattiello, Sara,Rooney, Myles,Sanzone, Alessandro,Brazzo, Paolo,Sassi, Mauro,Beverina, Luca

supporting information, p. 654 - 657 (2017/02/10)

Recently, oxygen-equilibrated water solutions of Kolliphor EL, a well-known surfactant, have been seen to form nanomicelles with oxygen-free cores. This has prompted the successful testing of the core environment as a green medium for palladium-catalyzed Suzuki-Miyaura cross couplings. The versatility of these conditions is endorsed by several examples, including the synthesis of relevant molecular semiconductors. The reaction medium can also be recycled, opening the way for an extremely easy and green chemistry compliant methodology.

Symmetric fluorenylbenzimidazole derivative and preparation method therefor

-

Paragraph 13, (2017/07/21)

The invention relates to a symmetric fluorenylbenzimidazole derivative and a preparation method therefor. The compound has a structural general formula represented by a formula shown in the description. The method is convenient, universal and economical. The compound has an extensive application prospect in the fields of organic photoelectric materials and fluorescence probing based analysis; in addition, the compound has a symmetrical structure, so that the molecular thermal stability of the compound is improved greatly, and the manufacturing of OLED (Organic Light Emitting Diode) light-emitting devices is better facilitated.

N-TYPE ORGANIC SEMICONDUCTORS INCLUDING AT LEAST TWO 2-DICYANOMETHYLENE-3-CYANO-2,5-DIHYDROFURAN GROUPS

-

Page/Page column 11-12, (2012/05/20)

The invention relates to a method for manufacturing transistors. Said method involves using a molecule including at least two 2-dicyanomethylene-3-cyano-2,5-dihydrofuran groups. The invention can be implemented in particular in the field of electronics.

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