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858661-74-2

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858661-74-2 Usage

Description

1H-Indazole-3-carbonitrile, 6-nitro-, also known as 6-nitro-1H-indazole-3-carbonitrile, is a chemical compound with the molecular formula C8H5N5O2. It is a nitro-substituted derivative of indazole, a bicyclic nitrogen-containing heterocycle. 1H-Indazole-3-carbonitrile, 6-nitrois characterized by the presence of a nitro group attached to the 6-position of the indazole ring and a carbonitrile group at the 3-position. Due to its unique structure and functional groups, 1H-Indazole-3-carbonitrile, 6-nitrohas potential applications in various fields, particularly in organic synthesis and pharmaceutical research.

Uses

Used in Organic Synthesis:
1H-Indazole-3-carbonitrile, 6-nitrois used as a building block in organic synthesis for the preparation of other chemical compounds. Its unique structure and functional groups make it a versatile starting material for the synthesis of various organic molecules.
Used in Pharmaceutical Research:
1H-Indazole-3-carbonitrile, 6-nitrois used in pharmaceutical research as a potential starting material for the development of new drugs or pharmaceuticals. The nitro group in this compound can be reduced or further modified to generate a range of biologically active molecules with potential therapeutic applications.
Used in Drug Development:
1H-Indazole-3-carbonitrile, 6-nitromay have potential applications in the development of new drugs or pharmaceuticals. Its unique structure and functional groups can be exploited to design and synthesize novel drug candidates with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 858661-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,6,6 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 858661-74:
(8*8)+(7*5)+(6*8)+(5*6)+(4*6)+(3*1)+(2*7)+(1*4)=222
222 % 10 = 2
So 858661-74-2 is a valid CAS Registry Number.

858661-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-cyano-6-nitroindazole

1.2 Other means of identification

Product number -
Other names -

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:858661-74-2 SDS

858661-74-2Relevant articles and documents

1H-INDAZOLES, BENZOTHIAZOLES, 1,2-BENZOISOXAZOLES, 1,2-BENZOISOTHIAZOLES, AND CHROMONES AND PREPARATION AND USES THEREOF

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Page/Page column 69-70, (2008/06/13)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nAChR), activation of nAChRs, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (indazoles and benzothiazoles), which act as ligands for the α7 nAChR subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

INDOLES, 1H-INDAZOLES, 1,2-BENZISOXAZOLES, AND 1,2-BENZISOTHIAZOLES, AND PREPARATION AND USES THEREOF

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Page/Page column 37, (2008/06/13)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nAChR), activation of nAChRs, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds for example, indoles, 1H-indazoles, 1,2-benzisoxazoles, and 1,2-benzisothiazoles, which act as ligands for the α7 nAChR subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

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