187148-77-2

Basic information

• Product Name: 9-(2-ETHYLHEXYL)CARBAZOLE 97
• Synonyms: 9-(2-ETHYLHEXYL)CARBAZOLE 97;9-(2-Ethylhexyl)carbazole 97%
• CAS NO: 187148-77-2
• Molecular Formula: C₂₀H₂₅N
• Molecular Weight: 279.424
• Product Categories: API intermediates;Building Blocks;Carbazoles;Heterocyclic Building Blocks
• Mol File: 187148-77-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 40 °C3 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 1.004 g/mL at 25 °C(lit.)
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: n20/D 1.5949(lit.)
• Water Solubility: Soluble in water
• CAS DataBase Reference: 9-(2-ETHYLHEXYL)CARBAZOLE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(2-ETHYLHEXYL)CARBAZOLE 97(187148-77-2)
• EPA Substance Registry System: 9-(2-ETHYLHEXYL)CARBAZOLE 97(187148-77-2)

Safety Data

• Hazard Codes: T
• Statements: 25-36/37/38
• Safety Statements: 26-36/37/39-45
• RIDADR: UN 2810 6.1/PG 3
• WGK Germany: 3
• Hazardous Substances Data: 187148-77-2(Hazardous Substances Data)

Usage

General Description

9-(2-ethylhexyl)carbazole 97 is a chemical compound with the molecular formula C24H29N. It is commonly used in the production of various substances such as dyes, pigments, and polymers. 9-(2-ETHYLHEXYL)CARBAZOLE 97 is known for its high purity of 97% and is often utilized in the manufacturing of organic semiconductors and organic photovoltaic devices. It has a wide range of applications in the field of electronics and is favored for its stability and reliability in a variety of processes. Additionally, it is also used in research and development activities due to its unique chemical properties and potential for various industrial applications.

InChI:InChI=1/C20H25N/c1-3-5-10-16(4-2)15-21-19-13-8-6-11-17(19)18-12-7-9-14-20(18)21/h6-9,11-14,16H,3-5,10,15H2,1-2H3

Upstream product

• 301-13-3 tris(2-ethylhexyl) phosphite 
• 86-00-0 2-nitrobiphenyl 

Downstream Products

• 169051-20-1 9-(2-ethylhexyl)-9H-carbazole-3,6-dicarbaldehyde 
• 173063-52-0 3,6-dibromo-9-(2-ethyl-hexyl)-9H-carbazole 
• 856422-39-4 2-bromo-9-(2-ethylhexyl)carbazole 
• 287978-28-3 9-(2-ethylhexyl)-9H-carbazole-3-carbaldehyde 
• 448955-87-1 9-(2-ethylhexyl)-3,6-bis(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-9H-carbazole 
• 856422-41-8 9-(2-ethylhexyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole 
• 628336-85-6 3-bromo-9-(2-ethylhexyl)-9H-carbazole 
• 1311143-99-3 C₃₉H₄₅NO₈ 
• 1311143-94-8 C₃₁H₃₃NO₄ 
• 1311143-93-7 [9-(2-ethyl-hexyl)-9H-carbazol-3-yl]-phenyl-methanone 

Relevant articles and documents

Efficient synthesis of N-alkyl-2,7-dihalocarbazoles by simultaneous carbazole ring closure and N-alkylation

The N-alkyl-2,7-dihalocarbazole as the main product was formed by the reaction of 4,4′-dihalo-2-nitrobiphenyl with aromatic nitro compound and trialkyl phosphite. The presence and crucial role of aromatic nitro compound causes simultaneous carbazole ring closure and N-alkylation unlike the Cadogan ring closure where non-alkylated carbazole is formed as a main product. In addition, the mixture of aromatic nitro compound and trialkyl phosphite was found to be a possible N-alkylating agent for heterocycles, such as carbazole or indole.