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7521-70-2

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7521-70-2 Usage

General Description

C-QUINOLIN-3-YL-METHYLAMINE, also known as 3-Quinoline-methylamine, is a chemical compound with the molecular formula C10H10N2. It is a derivative of quinoline, a heterocyclic aromatic compound. C-QUINOLIN-3-YL-METHYLAMINE is commonly used as an intermediate or building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It has potential applications in the development of new drugs and materials. The chemical structure of C-QUINOLIN-3-YL-METHYLAMINE consists of a quinoline ring with a methylamine group attached to the third carbon atom, giving it unique chemical and biological properties. Due to its versatile nature, C-QUINOLIN-3-YL-METHYLAMINE is the subject of ongoing research in various fields of chemistry and pharmaceutical science. Overall, it is an important compound in organic synthesis and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 7521-70-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,2 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7521-70:
(6*7)+(5*5)+(4*2)+(3*1)+(2*7)+(1*0)=92
92 % 10 = 2
So 7521-70-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2/c11-6-8-5-9-3-1-2-4-10(9)12-7-8/h1-5,7H,6,11H2

7521-70-2SDS

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 quinolin-3-ylmethanamine

1.2 Other means of identification

Product number -
Other names C-Quinolin-3-yl-methylamine

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:7521-70-2 SDS

7521-70-2Downstream Products

7521-70-2Relevant articles and documents

P2X3 AND/OR P2X2/3 COMPOUNDS AND METHODS

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Paragraph 0366-0369, (2018/04/17)

The present disclosure provides novel compounds and methods for preparing and using these compounds. In one embodiment, the compounds are of the structure of formula (I), wherein R1-R7 are defined herein. In a further embodiment, these compounds are useful in method for regulating one or both of the P2X3 or P2X2/3 receptors. In another embodiment, these compounds are useful for treating pain in patients by administering one or more of the compounds to a patient. In another embodiment, these compounds are useful for treating respiratory dysfunction in patients by administering one or more of the compounds to a patient.

6-O-SUBSTITUTED KETOLIDES HAVING ANTIBACTERIAL ACTIVITY

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Paragraph 0297; 0300, (2016/10/27)

PROBLEM TO BE SOLVED: To provide 6-O-substituted ketolides with antibacterial activity, having acid stability and enhanced activity toward gram negative bacteria and macrolide resistant gram positive bacteria. SOLUTION: This invention provides 6-O-substituted erythromycin ketolide derivatives such as formula (II) and compositions comprising the compounds. [Y and Z together form a group X; X is ketone, hydroxyimino or the like; or, one of Y and Z is H and the other is hydrogen, hydroxy or the like; Ra is H, hydroxy; Rc is H or a hydroxy protective group; R is a substituted methyl group]. COPYRIGHT: (C)2015,JPOandINPIT

PEPTIDE DEFORMYLASE INHIBITORS

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Page/Page column, (2014/02/15)

The present invention relates to a compound of Formula (I): or a pharmaceutically acceptable salt thereof, corresponding pharmaceutical compositions, compound preparation and treatment methods directed to bacterial infections and inhi-bition of bacterial peptide deformylase (PDF) activity

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