Welcome to LookChem.com Sign In|Join Free

CAS

  • or

23592-74-7

Post Buying Request

23592-74-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

23592-74-7 Usage

Description

2-ACETYLCARBAZOLE 98 is a monosubstituted carbazole derivative, which is a type of organic compound with a tricyclic structure consisting of two fused six-membered rings and one five-membered ring. It possesses potential larvicidal properties, making it a compound of interest for various applications.

Uses

Used in Pest Control Industry:
2-ACETYLCARBAZOLE 98 is used as a larvicide for controlling mosquito populations. Its larvicidal activity is particularly effective against mosquitoes, which are vectors for various diseases such as malaria, dengue, and Zika virus. By targeting the larval stage of mosquito development, 2-ACETYLCARBAZOLE 98 can help reduce the overall mosquito population and limit the spread of these diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 23592-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,9 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23592-74:
(7*2)+(6*3)+(5*5)+(4*9)+(3*2)+(2*7)+(1*4)=117
117 % 10 = 7
So 23592-74-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H11NO/c1-9(16)10-6-7-12-11-4-2-3-5-13(11)15-14(12)8-10/h2-8,15H,1H3

23592-74-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (649228)  2-Acetylcarbazole  98%

  • 23592-74-7

  • 649228-1G

  • 1,565.46CNY

  • Detail

23592-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(9H-carbazol-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-Carbazol-2-yl-aethanon

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:23592-74-7 SDS

23592-74-7Relevant articles and documents

2-Aminocarbazole synthesis

Kyziol,Lyzniak

, p. 3017 - 3019 (1980)

-

Self-Assembled Multilayer Iron(0) Nanoparticle Catalyst for Ligand-Free Carbon-Carbon/Carbon-Nitrogen Bond-Forming Reactions

Akiyama, Toshiki,Arisawa, Mitsuhiro,Haneoka, Hitoshi,Harada, Kazuo,Hasegawa, Jun-Ya,Honma, Tetsuo,Mashima, Kazushi,Sato, Yoshihiro,Shimoda, Shuhei,Shio, Yasunori,Suzuki, Takeyuki,Tamenori, Yusuke,Tsurugi, Hayato,Tsuruta, Kazuki,Wada, Yuki,Yamada, Makito

, p. 7244 - 7249 (2020/10/12)

Self-assembled multilayer iron(0) nanoparticles (NPs, 6-10 nm), namely, sulfur-modified Au-supported Fe(0) [SAFe(0)], were developed for ligand-free one-pot carbon-carbon/carbon-nitrogen bond-forming reactions. SAFe(0) was successfully prepared using a well-established metal-nanoparticle catalyst preparative protocol by simultaneous in situ metal NP and nanospace organization (PSSO) with 1,4-bis(trimethylsilyl)-1,4-dihydropyrazine (Si-DHP) as a strong reducing agent. SAFe(0) was easy to handle in air and could be recycled with a low iron-leaching rate in reaction cycles.

One-pot synthesis of carbazoles via tandem C-C cross-coupling and reductive amination

Goo, Deuk-Young,Woo, Sang Kook

supporting information, p. 122 - 130 (2015/12/30)

We have developed a highly efficient synthetic route to carbazoles that employs sequential C-C/C-N bond formation via Suzuki cross-coupling and Cadogan cyclization using commercially available or easily preparable starting materials. The developed method is compatible with electron neutral, rich or deficient substrates. The synthetic utility of this method was demonstrated by the concise syntheses of four natural products (glycozoline, glycozolicine, glycozolidine and clausenalene).

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 23592-74-7