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23043-41-6

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23043-41-6 Usage

General Description

1-methylacridine is a chemical compound with the molecular formula C13H11N. It is a derivative of acridine, a heterocyclic organic compound, and is commonly used as a building block in organic synthesis. 1-methylacridine has applications in the production of dyes, pharmaceuticals, and agrochemicals. It is known for its fluorescence properties and is used as a fluorescent tag in biological and chemical research. Additionally, 1-methylacridine has been investigated for potential anti-cancer and anti-microbial activities. However, it is important to handle and use 1-methylacridine with caution as it is a known irritant and may pose health risks if not properly handled.

Check Digit Verification of cas no

The CAS Registry Mumber 23043-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,4 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23043-41:
(7*2)+(6*3)+(5*0)+(4*4)+(3*3)+(2*4)+(1*1)=66
66 % 10 = 6
So 23043-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H11N/c1-10-5-4-8-14-12(10)9-11-6-2-3-7-13(11)15-14/h2-9H,1H3

23043-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methylacridine

1.2 Other means of identification

Product number -
Other names 1-Methyl-acridin

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:23043-41-6 SDS

23043-41-6Relevant articles and documents

Rh(III)-catalyzed synthesis of unsymmetrical acridines from aldehydes and azides using transient directing strategy in biomass-derived γ-valerolactone

Shen, Jun,Liu, Xi,Wang, Liang,Chen, Qun,He, Mingyang

, p. 1354 - 1362 (2018)

An Rh(III)-catalyzed synthesis of unsymmetrical acridines from aldehydes and azides through bilateral cyclization process in biomass-derived γ-valerolactone has been developed. The in situ-generated imino directing group (DG) from aldehyde and catalytic a

N-arylation of isatins

-

, (2008/06/13)

A process for the N-arylation of isatins with organo bismuth reagents is disclosed.

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