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1H-Imidazo[4,5-f]quinoline, 2-(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93201-91-3

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93201-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93201-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,0 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 93201-91:
(7*9)+(6*3)+(5*2)+(4*0)+(3*1)+(2*9)+(1*1)=113
113 % 10 = 3
So 93201-91-3 is a valid CAS Registry Number.

93201-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methylphenyl)-3H-imidazo[4,5-f]quinoline

1.2 Other means of identification

Product number -
Other names -

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:93201-91-3 SDS

93201-91-3Downstream Products

93201-91-3Relevant academic research and scientific papers

Studies on the Formation of Imidazoquinolines from Quinoline-5,6-diamine and Aromatic Aldehydes

Reddy, A. Pandu Ranga,Veeranagaiah, V.

, p. 372 - 376 (2007/10/02)

Condensation of quinoline-5,6-diamine (I) with aromatic aldehydes in acetic acid yields 3H-3-arylmethyl-2-imidazoquinolines (II) and 2-aryl-1H-imidazoquinolines (III).The formation of these compounds has been explained through the intermedia

A Facile Synthesis of 2-Substituted Imidazoquinolines

Reddy, A. Pandu Ranga,Veeranagaiah, V.

, p. 673 - 674 (2007/10/02)

Condensation of quinoline-5,6-diamine (II) with aliphatic and aromatic acids under catalytic and thermal conditions results in the corresponding 2-alkyl/aryl-1H-imidazoquinolines (I).

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