(6-Methoxy-quinolin-4-yl)-hydrazine

(6-Methoxy-quinolin-4-yl)-hydrazine Suppliers list
Company Name: SuZhou ShiYa Biopharmaceuticals, Inc.  
Tel: 0512-52358471 17715136450
Email: sales@shiyabiopharm.com
Products Intro: Product Name:(6-Methoxy-quinolin-4-yl)-hydrazine
CAS:49612-21-7
Purity:95% Package:1g;5g Remarks:B1-5555
Company Name: Interbioscreen Ltd.   
Tel: +7 (49) 6524-0091
Email: screen@ibscreen.chg.ru
Products Intro: CAS:49612-21-7
Package:10g Remarks:C10H11N3O
Company Name: PHARMEKS Ltd.   
Tel: +7 (495) 702-9648
Email: sales@pharmeks.com
Products Intro: Product Name:4-hydrazinyl-6-methoxyquinoline
CAS:49612-21-7
Package:10g
Company Name: Chemcia Scientific, LLC   
Tel: +1 (858) 678-0337
Email: sales@chemcia.com
Products Intro: Product Name:(6-Methoxy-quinolin-4-yl)-hydrazine
CAS:49612-21-7
Purity:0.95 Package:10g
(6-Methoxy-quinolin-4-yl)-hydrazine Basic information
Product Name:(6-Methoxy-quinolin-4-yl)-hydrazine
Synonyms:(6-Methoxy-quinolin-4-yl)-hydrazine;4-hydrazinyl-6-methoxyquinoline;Quinoline, 4-hydrazinyl-6-methoxy-
CAS:49612-21-7
MF:C10H11N3O
MW:189.21
EINECS:
Product Categories:
Mol File:49612-21-7.mol
(6-Methoxy-quinolin-4-yl)-hydrazine Structure
(6-Methoxy-quinolin-4-yl)-hydrazine Chemical Properties
Safety Information
MSDS Information
(6-Methoxy-quinolin-4-yl)-hydrazine Usage And Synthesis
Synthesis4-hydrazinyl-6-methoxyquinoline is prepared by reactig 4-chloro-6-methoxyquinoline and hydrazine monohydrate in the presence of concentrated hydrochloric acid.
Experiment steps:To a solution of 4-chloro-6-methoxyquinoline (579 mg, 4.78 mmol) and hydrazine monohydrate (442 mg, 5.74 mmol) in methanol (8 ml), concentrated hydrochloric acid (0.48 ml) was added dropwise. The reaction mixture was left to reflux overnight with stirring. After the reaction time, the reaction mixture was left to cool at room temperature. Upon cooling, the precipitate that formed was collected by filtration, dissolved in water and basified by the addition of saturated sodium hydroxide solution until pH 9. The aqueous layer was extracted using dichloromethane (3 × 15 ml), where the organic extracts were collected, dried using magnesium sulphate and concentrated in vacuo to give 4-hydrazinyl-6-methoxyquinoline as a waxy solid (200 mg, 22%).
(6-Methoxy-quinolin-4-yl)-hydrazine Preparation Products And Raw materials
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