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155014-05-4

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155014-05-4 Usage

General Description

5-Quinolinamine,3-fluoro-(9CI) is a chemical compound with the molecular formula C9H7FN. It belongs to the quinoline family and is characterized by the presence of a fluorine atom at the 3-position of the quinoline ring. 5-Quinolinamine,3-fluoro-(9CI) has potential applications in the field of pharmaceuticals and agrochemicals due to its unique structure and properties. It may be used as a building block in the synthesis of novel drugs and can also serve as a precursor for the development of new agrochemical products. The presence of the fluorine atom in its structure may also impart specific properties and biological activities that make it a valuable target for chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 155014-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,0,1 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 155014-05:
(8*1)+(7*5)+(6*5)+(5*0)+(4*1)+(3*4)+(2*0)+(1*5)=94
94 % 10 = 4
So 155014-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H7FN2/c10-6-4-7-8(11)2-1-3-9(7)12-5-6/h1-5H,11H2

155014-05-4SDS

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 3-fluoroquinolin-5-amine

1.2 Other means of identification

Product number -
Other names 3-Fluoro-5-aminoquinoline

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:155014-05-4 SDS

155014-05-4Relevant articles and documents

INHIBITORS OF JUN N-TERMINAL KINASE

-

Page/Page column 146, (2010/08/18)

The present disclosure provides inhibitors of c-Jun N-terminal kinases (JNK) having a structure according to the following formula (I): or a salt or solvate thereof, wherein ring A, Ca, Cb, Z, R5, W and Cy are defined herein. The disclosure further provides pharmaceutical compositions including the compounds of the present disclosure and methods of making and using the compounds and compositions of the present disclosure, e.g., in the treatment and prevention of various disorders, such as Alzheimer's disease.

Dual stimulatory and inhibitory effects of fluorine-substitution on mutagenicity: An extension of the enamine epoxide theory for activation of the quinoline nucleus

Saeki, Ken-Ichi,Kawai, Hiroshi,Kawazoe, Yutaka,Hakura, Atsushi

, p. 646 - 650 (2007/10/03)

Nineteen mono- and di-fluorinated derivatives of quinoline, 1,7- phenanthroline, 1,10-phenanthroline, benzo-[h]quinoline, and benzo[f]quinoline were subjected to analysis of their structure-mutagenicity relationships. For this purpose, six new fluorinated derivatives were synthesized. The results support that the enamine epoxide structure of the pyridine moiety, as well as the bay-region epoxide structure, is responsible for mutagenicity. Formation of K-region epoxides might involve a detoxification process rather than mutagenic activation.

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