574-39-0

Basic information

• Product Name: 9-ACETYLCARBAZOLE 97
• Synonyms: 9-ACETYLCARBAZOLE 97;NSC 39028;1-(9H-Carbazol-9-yl)ethanone
• CAS NO: 574-39-0
• Molecular Formula: C₁₄H₁₁NO
• Molecular Weight: 209.247
• Product Categories: Building Blocks;Carbazoles;Heterocyclic Building Blocks
• Mol File: 574-39-0.mol

Chemical Properties

• Melting Point: 77-79 °C(lit.)
• Boiling Point: 348.61°C (rough estimate)
• Flash Point: 144.6 °C
• Appearance: /
• Density: 1.1580
• Vapor Pressure: 0.000435mmHg at 25°C
• Refractive Index: 1.6400 (estimate)
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: soluble in Toluene
• CAS DataBase Reference: 9-ACETYLCARBAZOLE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 9-ACETYLCARBAZOLE 97(574-39-0)
• EPA Substance Registry System: 9-ACETYLCARBAZOLE 97(574-39-0)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 574-39-0(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
9-ACETYLCARBAZOLE 97 is used as a precursor in the synthesis of various organic compounds, contributing to the development of new chemical entities and materials.
Used in Pharmaceutical Research:
9-ACETYLCARBAZOLE 97 is utilized in pharmaceutical research for the development of new drugs and pharmaceutical products, potentially leading to advancements in medicinal chemistry.
Used in the Development of Organic Semiconductors:
As a derivative of carbazole, 9-ACETYLCARBAZOLE 97 is used in the development of organic semiconductors, which have applications in electronic devices, solar cells, and other technologies.
Used in Laboratory and Industrial Settings:
The 97% purity level of 9-ACETYLCARBAZOLE 97 ensures a high-quality and reliable source for use in both laboratory and industrial settings, facilitating research and production processes.

InChI:InChI=1/C14H11NO/c1-10(16)15-13-8-4-2-6-11(13)12-7-3-5-9-14(12)15/h2-9H,1H3

Upstream product

• 19591-17-4 o-iodoacetanilide 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 60-35-5 acetamide 
• 17763-95-0 2,2'-bis-<<(trifluoromethyl)sulfonyl>oxy>biphenyl 

Downstream Products

• 23592-69-0 1-(9H-carbazol-1-yl)ethan-1-one 
• 86-74-8 9H-carbazole 
• 10336-16-0 3-chloro-N-acetylcarbazole 
• 38573-63-6 9-acetyl-3,6-dibromocarbazole 
• 33633-88-4 1-(3,6-dichlorocarbazol-9-yl)ethanone 
• 64-19-7 acetic acid 
• 71-50-1 acetate 
• 3215-37-0 3-acetylcarbazole 
• 31438-22-9 1-nitro-9H-carbazole 
• 89672-04-8 1-(3-nitrocarbazol-9-yl)ethanone 
• 3244-54-0 3,6-dinitro-9H-carbazole 
• 14191-22-1 2-nitrocarbazole 
• 3077-85-8 3-Nitro-carbazol 
• 674-82-8 4-methyleneoxetan-2-one 

Relevant articles and documents

Synthesis of N-acylcarbazoles through palladium-catalyzed aryne annulation of 2-haloacetanilides

N-Acylcarbazoles have been synthesized in moderate to good yields by the annulation of in situ generated arynes with 2-haloacetanilides in the presence of a palladium catalyst and CsF. Both C-C and C-N bonds are formed simultaneously, and a variety of fun

Double N-arylation of primary amines: Carbazole synthesis from 2,2′-biphenyldiols

(Chemical Equation Presented) The double N-arylation of primary amines with 2,2′-biphenylylene ditriflates was investigated for the synthesis of multisubstituted carbazoles. Palladium complexes supported by 2-dicyclohexylphosphino-2′-methylbiphenyl or Xantphos [4,5- bis(diphenylphosphino)-9,9-dimethylxanthene] were found to be efficient catalysts for the reaction. The catalysts allow the use of anilines with an electron-donating or electron-withdrawing substituent and multisubstituted 2,2′-biphenylylene ditriflates as substrates. Ammonia equivalents, such as O-tert-butyl carbamate, are also employable as a nitrogen source to give the N-protected carbazoles which can easily give the corresponding N-unsubstituted carbazoles after deprotection. By using this methodology, a carbazole alkaloid, mukonine, is synthesized in 40% yield for five steps, in comparable efficiency to the recent precedents.