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9-Benzyl-3-bromocarbazole is a chemical compound with the molecular formula C20H14BrN. It is a brominated derivative of carbazole, featuring a benzyl group attached to the 9th position and a bromine atom at the 3rd position of the carbazole ring. 9-Benzyl-3-bromocarbazole is recognized for its interactions with biological systems, making it a candidate for drug design and development. It also exhibits intriguing photophysical properties, which have been explored for applications in optoelectronic devices. With its diverse potential uses, 9-Benzyl-3-bromocarbazole is significant in the realms of chemistry, pharmacology, and materials science.

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  • 339576-55-5 Structure
  • Basic information

    1. Product Name: 9-Benzyl-3-bromocarbazole
    2. Synonyms: 9-Benzyl-3-bromocarbazole;9-Benzyl-3-bromo-9H-carbazole
    3. CAS NO:339576-55-5
    4. Molecular Formula: C19H14BrN
    5. Molecular Weight: 336.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 339576-55-5.mol
  • Chemical Properties

    1. Melting Point: 116.0 to 120.0 °C
    2. Boiling Point: 500.0±37.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.35±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 9-Benzyl-3-bromocarbazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9-Benzyl-3-bromocarbazole(339576-55-5)
    11. EPA Substance Registry System: 9-Benzyl-3-bromocarbazole(339576-55-5)
  • 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: 339576-55-5(Hazardous Substances Data)

339576-55-5 Usage

Uses

Used in Pharmaceutical Research:
9-Benzyl-3-bromocarbazole is utilized as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique structural features and reactivity. Its ability to interact with biological systems positions it as a valuable component in drug design, potentially leading to the development of new therapeutic agents.
Used in Organic Synthesis:
As a brominated derivative of carbazole, 9-Benzyl-3-bromocarbazole serves as a versatile building block in organic synthesis. Its presence in the synthesis of complex organic molecules can contribute to the creation of novel chemical entities with specific properties and applications.
Used in Optoelectronic Devices:
9-Benzyl-3-bromocarbazole is employed in the development of optoelectronic devices due to its photophysical properties. Its potential use in this industry could include the creation of advanced materials for applications such as solar cells, light-emitting diodes (LEDs), and other photonic technologies.
Used in Materials Science:
9-Benzyl-3-bromocarbazole's unique chemical structure and properties make it a candidate for use in the development of new materials with specific characteristics. This can include materials with tailored electronic, optical, or mechanical properties for use in various high-tech applications.

Check Digit Verification of cas no

The CAS Registry Mumber 339576-55-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,5,7 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 339576-55:
(8*3)+(7*3)+(6*9)+(5*5)+(4*7)+(3*6)+(2*5)+(1*5)=185
185 % 10 = 5
So 339576-55-5 is a valid CAS Registry Number.

339576-55-5SDS

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 9-Benzyl-3-bromo-9H-carbazole

1.2 Other means of identification

Product number -
Other names 5-[Bis(2-chloroethyl)amino]-1-methylbenzimidazole-2-butyric Acid Hydrochloride Hydrate

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:339576-55-5 SDS

339576-55-5Downstream Products

339576-55-5Relevant articles and documents

Synthesis and electronic spectroscopy of bromocarbazoles. Direct bromination of N- and C-substituted carbazoles by N-bromosuccinimide or a N-bromosuccinimide/silica gel system

Ponce, Maria B.,Cabrerizo, Franco M.,Bonesi, Sergio M.,Erra-Balsells, Rosa

, p. 1123 - 1139 (2006)

The preparation, isolation and characterization by elemental analysis and 1H-NMR, 13C-NMR, and MS data of the bromo derivatives of N-substituted carbazoles, i.e., of 9-methyl-9H-carbazole (1), 9-phenyl-9H-carbazole (2), 9-benzyl-9H-carbazole (3), 2-methoxy-9-methyl-9H- carbazole (4), and of C-substituted carbazoles, i.e., of 2-(acetyloxy)-9H- carbazole (5) and 3-nitro-9H-carbazole (6), are reported, in part for the first time. As brominating reagents, N-bromosuccinimide (NBS) or NBS/silica gel in CH2Cl2, NBS in AcOH, KBrO3/KBr in EtOH doped with a catalytic amount of H2SO4, or KBrO3/KBr in AcOH were employed, and their uses were compared. Semi-empirical PM3 calculations were performed to predict the reactivity of the N-substituted and C-substituted carbazoles and of their bromo derivatives and found to verify the experimental results. The UV-absorption and fluorescence and phosphorescence emission spectra of the bromocarbazole derivatives in MeCN solution at 298 K and in a solid matrix at 77 K were compared with those of the corresponding carbazoles 1-6. The dynamic properties of the lowest excited singlet and triplet states (τf, τp, φf, and φp) were measured under the same experimental conditions. The intramolecular spin-orbital-coupling effect of the Br-atom and NO2 group on the spectroscopic data, photophysical parameters, and on the photo reactivity were also briefly analyzed.

COMPOUND FOR ORGANIC ELECTROLUMINESCENT DEVICE AND ORGANIC ELECTROLUMINESCENT DEVICE HAVING THE SAME

-

, (2012/01/12)

The present invention provides a compound of formula (I) for an organic electroluminescent device: wherein X and Y are each independently selected for the group consisting of an alkyl substituted, aryl substituted or unsubstituted carbazole, indolocarbazole, triphenylsilyl and diphenylphosphine oxide represented by formula (A), (B), (C), (D) or (E), in which R1, R2, and R3 are each independently selected from the group consisting of a hydrogen, an alkyl having 1 to 15 carbons atoms, an aryl group having 6 to 15 carbons atoms, an alkyl substituted, an aryl substituted or unsubstituted triphenylsilyl, and a diphenylphosphine oxide represented by the formula (D) or (E); m and n are each independently 0 or 1, provided that m+n is 1 or more; and Ar1 and Ar2 are each independently selected from the group consisting of an alkyl substituted, aryl substituted or unsubstituted phenyl, tolyl, naphthyl, fluorenyl, anthracenyl, and phenanthryl.

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