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4-Methyl-6-nitroindazole, a nitroimidazole derivative with the molecular formula C9H8N4O2, is a pale yellow solid that is insoluble in water but soluble in organic solvents. It belongs to the class of organic compounds known as nitroimidazoles and is commonly used as a building block for the synthesis of other organic compounds, particularly in the pharmaceutical and agrochemical industries. The presence of a nitro group in the molecule makes it a useful precursor for various synthetic applications.

885520-77-4

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885520-77-4 Usage

Uses

Used in Pharmaceutical Industry:
4-Methyl-6-nitroindazole is used as a building block for the synthesis of pharmaceuticals due to its unique chemical structure and properties. Its presence as a nitroimidazole derivative allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 4-Methyl-6-nitroindazole is utilized as a precursor for the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural chemicals.
Used in Imaging Agents for PET Scans:
4-Methyl-6-nitroindazole has been studied for its potential use in imaging agents for positron emission tomography (PET) scans. Its unique properties make it a promising candidate for the development of new imaging agents that can enhance the diagnostic capabilities of PET scans in various medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 885520-77-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,5,2 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 885520-77:
(8*8)+(7*8)+(6*5)+(5*5)+(4*2)+(3*0)+(2*7)+(1*7)=204
204 % 10 = 4
So 885520-77-4 is a valid CAS Registry Number.

885520-77-4SDS

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 1H-Indazole, 4-methyl-6-nitro-

1.2 Other means of identification

Product number -
Other names 4-Methyl-6-nitroindazle

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:885520-77-4 SDS

885520-77-4Downstream Products

885520-77-4Relevant academic research and scientific papers

2-AMINOQUINAZOLINE DERIVATIVE

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Page/Page column 42, (2010/09/17)

An object of the present invention is to provide compounds which are useful as protein kinase inhibitors. Disclosed is a 2-aminoquinazoline derivative represented by the following formula (I): wherein R1 represents a lower alkyl group which may be substituted with a halogen atom, or a halogen atom; R2 represents a hydrogen atom, a substituted or unsubstituted lower alkyl group, a halogen atom, a hydroxyl group, a substituted or unsubstituted lower alkoxy group, a substituted or unsubstituted amino group, a substituted or unsubstituted acylamino group, a carboxyl group, a lower alkoxycarbonyl group, a carbamoyl group, or a substituted or unsubstituted lower alkylureido group; and X, Y and Z each independently represents a hydrogen atom, a substituted or unsubstituted lower alkyl group, a halogen atom, a hydroxyl group, a carboxyl group, a lower alkoxycarbonyl group, a cyano group, a carbamoyl group, a substituted or unsubstituted lower alkoxy group, a substituted or unsubstituted amino group, a substituted or unsubstituted lower alkoxycarbonylamino group, a substituted or unsubstituted lower alkylaminocarbonyl group, a lower alkylsulfonylamino group, a substituted or unsubstituted lower alkylureido group, or a substituted or unsubstituted acylamino group, or X and Y may be combined to form a 5- to 6-membered ring forming a bicyclic fused ring, wherein the 5- to 6-membered ring may optionally have a substituent, provided that when X and Y are not combined to form a fused ring, R2 represents a hydrogen atom and, when X and Y are combined to form a fused ring, a saturated or unsaturated, bicyclic alicyclic or heterocyclic fused ring can be formed.

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