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3-(2-Morpholinoethoxy)-1H-indazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36173-90-7

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36173-90-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36173-90-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,7 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36173-90:
(7*3)+(6*6)+(5*1)+(4*7)+(3*3)+(2*9)+(1*0)=117
117 % 10 = 7
So 36173-90-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H17N3O2.BrH/c1-2-4-12-11(3-1)13(15-14-12)18-10-7-16-5-8-17-9-6-16;/h1-4H,5-10H2,(H,14,15);1H

36173-90-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(1H-indazol-3-yloxy)ethyl]morpholine

1.2 Other means of identification

Product number -
Other names 3-(2-morpholin-4-yl-ethoxy)-1(2)H-indazole

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:36173-90-7 SDS

36173-90-7Upstream product

36173-90-7Downstream Products

36173-90-7Relevant academic research and scientific papers

Analgesic compositions comprising 1H- or respectively 2H-indazolone-3 (β-morpholino-alkoxy) compounds

-

, (2008/06/13)

A process of producing 1H- or respectively 2H-indazolone-3, particularly 3-(β-morpholino-ethoxy)-1H-indazole, 3-(γ-morpholino-propoxy)-1H-indazole and the novel chemical compound 3-(β-morpholino-ethoxy)-4,5,6,7-tetrahydro-2H-indazole by reacting the enolate of 1H-indazolone-3 with morpholino-ethyl-chloride or respectively with γ-morpholino-propyl-chloride, or by reacting the enolate of 4,5,6,7-tetrahydro-2H-indazolone-3 with β-morpholino-ethyl-chloride, under well-defined conditions, resulting in higher yields and optimum purity.

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