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574-39-0

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574-39-0 Usage

General Description

9-ACETYLCARBAZOLE 97 is a chemical compound with a purity of 97%, primarily used in the field of organic synthesis and pharmaceutical research. It is a derivative of carbazole, a heterocyclic aromatic compound with potential applications in the development of organic semiconductors and as a precursor in the synthesis of various organic compounds. The 97% purity level ensures a high-quality and reliable source of 9-ACETYLCARBAZOLE for use in laboratory and industrial settings. Additionally, this compound may have potential applications in the development of new drugs and pharmaceutical products.

Check Digit Verification of cas no

The CAS Registry Mumber 574-39-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 574-39:
(5*5)+(4*7)+(3*4)+(2*3)+(1*9)=80
80 % 10 = 0
So 574-39-0 is a valid CAS Registry Number.
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

574-39-0 Well-known Company Product Price

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  • Aldrich

  • (649201)  9-Acetylcarbazole  97%

  • 574-39-0

  • 649201-1G

  • 1,283.49CNY

  • Detail

574-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-carbazol-9-ylethanone

1.2 Other means of identification

Product number -
Other names 9-Acetyl-carbazol

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:574-39-0 SDS

574-39-0Relevant articles and documents

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

Lu, Chun,Markina, Nataliya A.,Larock, Richard C.

, p. 11153 - 11160 (2013/02/22)

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

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