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5-HYDRAZINOQUINOLINE DIHYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91004-60-3

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91004-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91004-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,0 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91004-60:
(7*9)+(6*1)+(5*0)+(4*0)+(3*4)+(2*6)+(1*0)=93
93 % 10 = 3
So 91004-60-3 is a valid CAS Registry Number.

91004-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name quinolin-5-ylhydrazine,dihydrochloride

1.2 Other means of identification

Product number -
Other names 5-quinolylhydrazine dihydrochloride

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:91004-60-3 SDS

91004-60-3Relevant academic research and scientific papers

The synthesis of 4-(3,3-dimethyl-3H-pyrrolo[2,3-f] quinolin-2-yl)pyrazoles and 4-(3,3-dimethyl-3H-pyrrolo[3,2-h] quinolin-2-yl)pyrazoles

Rashidi,Afghan,Baradarani, Mehdi M.,Jouleb, John A.

body text, p. 428 - 431 (2009/09/25)

(Chemical Equation Presented) 5-Hydrazinoquinoline and 8-hydrazinoquinoline were converted via Fischer syntheses with 3-methylbutan-2-one into pyrido-indolenines 2,3,3-trimethyl-3H-pyrrolo[2,3-f]quinoline 7 and 2,3,3-trimethyl-3H-pyrrolo[ 3,2-h]quinoline 11, respectively. Exposure of the indolenines to the Vilsmeier reagent produced aminomethylene-malondialdehydes 8 and 12, which reacted with hydrazine or arylhydrazines to give 4-(3H-pyrrolo[2,3-f]quinolin-2-yl)- and 4-(3H-pyrrolo[3,2-h]quinolin-2-yl)- pyrazoles, 9 and 13.

Structure-activity relationship studies on N′-aryl carbohydrazide P2X7 antagonists

Nelson, Derek W.,Sarris, Kathy,Kalvin, Douglas M.,Namovic, Marian T.,Grayson, George,Donnelly-Roberts, Diana L.,Harris, Richard,Honore, Prisca,Jarvis, Michael F.,Faltynek, Connie R.,Carroll, William A.

experimental part, p. 3030 - 3034 (2009/04/10)

N′-Aryl acyl hydrazides were identified as P2X7 receptor antagonists. Structure-activity relationship (SAR) studies evaluated functional activity by monitoring calcium flux inhibition in cell lines expressing recombinant human and rat P2X7 receptors. Selected analogs were assayed in vitro for their capacity to inhibit release of cytokine IL-1β. Compounds with potent antagonist function were evaluated in vivo using the zymosan-induced peritonitis model. A representative compound effectively attenuated mechanical allodynia in a rat model of neuropathic pain.

ACYLHYDRAZIDE P2X7 ANTAGONISTS AND USES THEREOF

-

Page/Page column 42-43, (2008/06/13)

The present invention discloses a compound of formula (I) or a pharmaceutically acceptable salt or prodrug thereof, wherein D, A, m, n, Rx and Ry are defined in the description. The present invention also relates to pharmaceutical compositions of compound

METHODS FOR PREPARING SODIUM-HYDROGEN EXCHANGER TYPE-1 INHIBITORS

-

, (2008/06/13)

This invention relates to methods of preparing sodium-hydrogen exchanger type 1 (NHE-1) inhibitors of formula I′ and methods of preparing pharmaceutical compositions comprising such NHE-1 inhibitors.

Preparation of sodium-hydrogen exchanger type-1 inhibitors

-

, (2008/06/13)

This invention relates to methods of preparing sodium-hydrogen exchanger type 1 (NHE-1) inhibitors of formula I′ 1intermediates of the NHE-1 inhibitors and a new almost colorless form of the NHE-1 inhibitor N-(5-cyclopropyl-1-quinolin-5-yl-1H-pyrazole-4-carbonyl)-guanidine.

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