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750573-26-3

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750573-26-3 Usage

General Description

9-(3,5-Dibromophenyl)-9H-carbazole is a chemical compound with the molecular formula C18H10Br2N. It is a carbazole derivative that contains two bromine atoms and a 3,5-dibromophenyl group. 9-(3,5-Dibromophenyl)-9H-carbazole is commonly used in organic synthesis, particularly in the development of organic optoelectronic materials and as a component in various pharmaceuticals. It exhibits a wide range of applications including its use as a precursor in the construction of organic light-emitting diodes (OLEDs) and as a building block in the synthesis of polymers for organic solar cells. Additionally, it has been studied for its potential anti-cancer and antiviral properties, making it a versatile and important compound in both the chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 750573-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,0,5,7 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 750573-26:
(8*7)+(7*5)+(6*0)+(5*5)+(4*7)+(3*3)+(2*2)+(1*6)=163
163 % 10 = 3
So 750573-26-3 is a valid CAS Registry Number.

750573-26-3 Well-known Company Product Price

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  • TCI America

  • (D4978)  9-(3,5-Dibromophenyl)carbazole  >98.0%(GC)

  • 750573-26-3

  • 200mg

  • 790.00CNY

  • Detail
  • TCI America

  • (D4978)  9-(3,5-Dibromophenyl)carbazole  >98.0%(GC)

  • 750573-26-3

  • 1g

  • 2,990.00CNY

  • Detail

750573-26-3SDS

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 9-(3,5-dibromophenyl)carbazole

1.2 Other means of identification

Product number -
Other names Triethylenediamine

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:750573-26-3 SDS

750573-26-3Downstream Products

750573-26-3Relevant articles and documents

Metal-nickel complex and preparation method and application thereof

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Paragraph 0054-0056; 0060; 0077-0078; 0087-0088, (2022/01/12)

The present invention discloses a metal-nickel complex and preparation method and application thereof. The metal nickel complex having a structure shown in Formula I below, wherein:R1 each time it appears, each time independently selected from C1-10 alkyl, -C1-6 alkyl-C 6-12 aryl, C6-12 aryl-C1-6 alkyl;P1,P2 Each time it appears, each independently selected from H, halogen, C1-6 alkyl, C2-6 enyl, C3-20 aryl, C3-20 heteroaryl, and whenP1,P2 are not H or halogen, adjacentP1,P2 Energy bond synthesis ring; D is the electron-absorbing group; A is the electron-absorbing group. This metal-nickel complex has good fluorescence luminescence performance.

A germanium-containing organic electroluminescent material and its organic light-emitting device

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Paragraph 0054; 0055; 0056, (2018/07/07)

The present invention provides a germanium-containing organic electroluminescent material and its organic light-emitting device, which belongs to the technical field of organic photoelectric material. The present invention provides a germanium-containing

Organic compound with long afterglow effect as well as preparation method and application of organic compound

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Paragraph 0042; 0043; 0044; 0045, (2017/07/21)

The invention discloses an organic compound with a long afterglow effect as well as a preparation method and application of the organic compound. The organic compound has a structural formula as follows: the formula is shown in the description; 9-phenylcarbazole with n-pi* is used as a basic unit, and a meta-position and a para-position of phenyl are modified; after modification, different 9-phenylcarbazole derivatives are obtained; a test shows that the fluorescence lifetime of the compound can reach 100ms or more. The compound provided by the invention has the characteristics of simple synthesis method, easiness of being purified, adjustable luminescent spectrum, flexibility, no need of doping inorganic rare-earth materials, cheap price, low toxicity and the like, and can be widely to various fields including biological imaging, disease diagnosis, optical counterfeiting prevention and the like.

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