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108099-80-5

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108099-80-5 Usage

Structure

2(1H)-Quinolinone core with a 6-fluoro group, 4-methyl group, and a hydrazone functional group.

Derivative

It is a hydrazone derivative of 6-fluoro-4-methylquinolin-2(1H)-one.

Usage

Building block for the synthesis of other compounds in chemical and pharmaceutical research.

Potential applications

Medicinal chemistry (requires further research to understand its potential uses and properties)

Importance

An important chemical compound with potential applications in various scientific and industrial fields.

Check Digit Verification of cas no

The CAS Registry Mumber 108099-80-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,0,9 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 108099-80:
(8*1)+(7*0)+(6*8)+(5*0)+(4*9)+(3*9)+(2*8)+(1*0)=135
135 % 10 = 5
So 108099-80-5 is a valid CAS Registry Number.

108099-80-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-fluoro-2-hydrazino-4-methylquinoline

1.2 Other means of identification

Product number -
Other names (6-Fluoro-4-methyl-quinolin-2-yl)-hydrazine

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:108099-80-5 SDS

108099-80-5Relevant articles and documents

Synthesis of Some 2-(3',5'-Dimethylpyrazol-1'-yl)-4-methyl-6-substituted-quinolines and Their 4'-Substituted Analogues

Singh, S. P.,Vaid, R. K.,Prakash, I.,Prakash, O.

, p. 945 - 950 (2007/10/02)

The reaction of 2-hydrazinoquinolines (2) with pentane-2,4-dione yields pyrazoles (1) instead of the reported diazepines (3).The structural assignment is based on a rigorous spectral analysis of the product and on unambiguous synthesis.Several pyrazolylquinolines (1, 6 and 7) bearing a variety of substituents were synthesized and evaluated for their antiinflammatory and antimalarial activities.

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