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3-Bromo-7-amino (1H)indazole is a heterocyclic aromatic compound that belongs to the indazole class. It features a unique structure with a bromine atom and an amino group attached to the indazole ring, which may confer specific properties and reactivity. This chemical compound holds potential for applications in organic synthesis, medicinal chemistry, and pharmaceutical research due to its distinctive characteristics and therapeutic possibilities.

316810-90-9

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316810-90-9 Usage

Uses

Used in Organic Synthesis:
3-Bromo-7-amino (1H)indazole is used as a building block in organic synthesis for the creation of more complex organic compounds. Its bromine and amino functional groups provide unique reactivity that can be exploited in various chemical reactions to form a wide range of products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-Bromo-7-amino (1H)indazole is utilized as a potential therapeutic agent. Its structure may offer opportunities for the development of new drugs targeting various diseases and conditions, making it a valuable candidate for further research and development.
Used in Pharmaceutical Research:
3-Bromo-7-amino (1H)indazole is employed in pharmaceutical research as a compound of interest for its potential applications in drug discovery. The presence of bromine and amino groups may contribute to its pharmacological properties, guiding its use in the treatment of specific medical conditions.
Used in Scientific and Industrial Contexts:
3-Bromo-7-amino (1H)indazole is also used in various scientific and industrial applications due to the specific properties imparted by its functional groups. Its reactivity and structural features make it a subject of interest for further study and potential use in a range of contexts beyond the realms of medicine and organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 316810-90-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,6,8,1 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 316810-90:
(8*3)+(7*1)+(6*6)+(5*8)+(4*1)+(3*0)+(2*9)+(1*0)=129
129 % 10 = 9
So 316810-90-9 is a valid CAS Registry Number.

316810-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-2H-indazol-7-amine

1.2 Other means of identification

Product number -
Other names 3-Bromo-1H-indazol-7-amine

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:316810-90-9 SDS

316810-90-9Downstream Products

316810-90-9Relevant academic research and scientific papers

Research in 7-aminoindazole series: Synthesis of new halo-7H-4-methylpyrazolo[1,5,4-ef][1,5]benzodiazepin-6-ones and 5H-9-halo-6-methylpyrazolo[1,5,4-ef][1,5]benzodiazepin-4-ones

Rakib,Benchidmi,Essassi,El Bouadili,Ibn Mansour,Bellan,Lopez,Lamande

, p. 339 - 345 (2007/10/03)

A new class of 7-aminohaloindazoles has been synthesized. Reactivity of the amino groups of these bicyclic systems has been investigated. The halogenated pyrazolo-1,5-benzodiazepinones have been synthesized by the condensation of 7-aminoindazoles with ethyl acetoacetate.

Reactivity of 7-aminoindazole as a bidendate nucleophile

Rakib, El Mostapha,Benchidmi, Mohammed,Essassi, El Mokhtar,Bouadili, Abdelaziz El,Khouili, Mostafa,Visseaux, Mark,Pujol, M.Dolors

, p. 2617 - 2627 (2007/10/03)

A simple route for the preparation of two new classes of heterocyclic systems: halopyrazolo[4,5-h]quinolines and halopyrazolo[1,5,4-ef][1,5]benzodiazepines, is presented. The effect of the solvent and the reactivity of pyrazolo-1,5-benzodiazepine were studied.

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