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2-(9H-carbazol-9-yl)benzoic acid is a chemical compound with the molecular formula C18H13NO2. It is a derivative of benzoic acid, featuring a carbazole moiety attached to the 2-position of the benzene ring. Carbazole is a tricyclic aromatic compound with a structure that includes two benzene rings fused to a pyrrole ring. 2-(9H-carbazol-9-yl)benzoic acid is known for its potential applications in the synthesis of various organic compounds and materials, such as dyes, pharmaceuticals, and光电材料. It is also recognized for its fluorescent properties, which can be exploited in the development of sensors and imaging technologies. The compound's structure endows it with unique electronic and optical characteristics, making it a subject of interest in materials science and organic chemistry research.

6286-88-0

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6286-88-0 Usage

Type of compound

Chemical compound

Derivative of

Benzoic acid

Contains

Carbazole group

Carbazole group structure

Fused heterocyclic compound composed of two six-membered rings and a five-membered ring

Potential applications

Organic synthesis and material science

Unique structure

Contributes to its potential applications

Possible use in

Development of organic electronic devices

Examples of organic electronic devices

Organic light-emitting diodes (OLEDs) and organic photovoltaic cells

Potential properties for devices

Electron transport and semiconducting properties

Additional applications

Pharmaceuticals and agrochemicals

Role in pharmaceuticals and agrochemicals

Potential for biological activity and synthesis of complex organic compounds

Check Digit Verification of cas no

The CAS Registry Mumber 6286-88-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6286-88:
(6*6)+(5*2)+(4*8)+(3*6)+(2*8)+(1*8)=120
120 % 10 = 0
So 6286-88-0 is a valid CAS Registry Number.

6286-88-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-carbazol-9-ylbenzoic acid

1.2 Other means of identification

Product number -
Other names 2-carbazol-9-yl-benzoic acid

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:6286-88-0 SDS

6286-88-0Relevant academic research and scientific papers

Hydrogen bonding boosted the persistent room temperature phosphorescence of pure organic compounds for multiple applications

Zhang, Tingting,Gao, Heqi,Lv, Anqi,Wang, Ziyi,Gong, Yongyang,Ding, Dan,Ma, Huili,Zhang, Yongming,Yuan, Wang Zhang

, p. 9095 - 9101 (2019)

Persistent room temperature phosphorescence (p-RTP) of pure organic compounds is drawing much attention due to its unique advantages and promising applications in anticounterfeiting, encryption, bioimaging, etc. Achieving efficient p-RTP, however, remains

Dual Gas-responsive Fluorescent Diblock Copolymer Synthesized via RAFT Polymerization

Zhang, Xiaozhen,Wang, Jinjin,Zhou, Shijia,Sun, Shuangshuang,Wang, Xiaorong,Guo, Shengwei,Zhao, Fengyang

, p. 435 - 442 (2022/01/24)

Stimulus-responsive polymers with luminescence properties have a wide range of applications in the fields of controlled drug release, fluorescent probes, and biological stents. In this paper, carbon dioxide (CO2)/oxygen (O2) dual-res

PYRROL-1 -YL BENZOIC ACID DERIVATES USEFUL AS MYC INHIBITORS

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Paragraph 00340, (2014/05/24)

The present invention provides compounds of Formula (I-A), (I-B), and (I-C), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting Myc (e.g., c-Myc) activity. The p

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