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(3-aminoquinolin-2-yl)methanol is a chemical compound with the molecular formula C10H10N2O. It is a derivative of quinoline, a heterocyclic aromatic compound that is commonly found in certain plants and is used in the production of dyes, drugs, and pesticides. (3-aminoquinolin-2-yl)methanol has a quinoline ring structure with an amino group and a hydroxyl group attached to it.
Used in Pharmaceutical Industry:
(3-aminoquinolin-2-yl)methanol is used as a building block for the synthesis of various bioactive compounds, including potential drug candidates. The presence of the amino and hydroxyl groups also gives it the potential to participate in chemical reactions to form new compounds with diverse properties.

75353-61-6

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75353-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75353-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,5 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75353-61:
(7*7)+(6*5)+(5*3)+(4*5)+(3*3)+(2*6)+(1*1)=136
136 % 10 = 6
So 75353-61-6 is a valid CAS Registry Number.

75353-61-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name amino-3 hydroxymethyl-2 quinoleine

1.2 Other means of identification

Product number -
Other names 3-amino-2-hydroxymethylquinoline

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:75353-61-6 SDS

75353-61-6Downstream Products

75353-61-6Relevant academic research and scientific papers

Design, synthesis, and structure-activity relationship studies of new phenolic DNA gyrase inhibitors

Luebbers, Thomas,Angehrn, Peter,Gmuender, Hans,Herzig, Silvia

, p. 4708 - 4714 (2008/02/10)

Starting from a biased needle screening hit 3a, we report herein the design and synthesis of a series of novel 2,3-dihydroisoindol-1-ones structurally related to cyclothialidine 2 with DNA gyrase inhibitory activity. In this series, some compounds exhibit

Sur les orthoamino formyl quinoleines, nouveaux synthons heterocycliques

Godard, Alain,Queguiner, Guy

, p. 465 - 473 (2007/10/02)

Les quatre orthoamino formyl quinoleines substituees sur le cycle pyridinique ont ete synthetisees par oxydation des amino hydroxymethyl quinoleines correspondantes.Parmi toutes les methodes envisagees, seule cette derniere a permis la preparation de l'amino-3 formyl-2 quinoleine, compose relativement peu stable.Ces nouveaux composes bifonctionnels derives de la qunoleine constituent des synthons particulierement interessants pour l'elaboration de certains heterocycles.

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