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5-Bromo-6-fluoroindoline-2,3-dione, a heterocyclic compound with the molecular formula C8H3BrFNO2, features a five-membered ring with two nitrogen atoms and two carbonyl groups. This versatile chemical intermediate is characterized by its unique structure and properties, making it an important compound in various industrial and research applications.

118897-99-7

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118897-99-7 Usage

Uses

Used in Pharmaceutical Synthesis:
5-Bromo-6-fluoroindoline-2,3-dione serves as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Synthesis:
5-broMo-6-fluoroindoline-2,3-dione is also utilized as an intermediate in the production of agrochemicals, playing a crucial role in the creation of effective pesticides and other agricultural products.
Used in Organic Synthesis:
5-Bromo-6-fluoroindoline-2,3-dione is employed in organic synthesis, where its unique structure and properties enable the development of novel organic compounds for various applications.
Used in Material Science:
In the field of material science, 5-broMo-6-fluoroindoline-2,3-dione has been investigated for its potential use in creating new materials with specific properties, such as improved stability or reactivity.
Used in Biological Research:
5-Bromo-6-fluoroindoline-2,3-dione has been studied for its potential biological activities, including anti-inflammatory and antifungal properties, making it a promising candidate for further research in the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 118897-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,8,9 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 118897-99:
(8*1)+(7*1)+(6*8)+(5*8)+(4*9)+(3*7)+(2*9)+(1*9)=187
187 % 10 = 7
So 118897-99-7 is a valid CAS Registry Number.

118897-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-6-fluoro-1H-indole-2,3-dione

1.2 Other means of identification

Product number -
Other names 5-Brom-6-fluor-indolin-2,3-dion

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:118897-99-7 SDS

118897-99-7Relevant academic research and scientific papers

SYK INHIBITOR AND USE METHOD THEREFOR

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, (2020/05/07)

Provided are a Syk inhibitor and a use method therefor, and in particular, disclosed are quinolinone represented by formula (I) or quinazoline derivatives or pharmaceutically acceptable salts thereof, a preparation method, a pharmaceutical composition, and uses in preparing a medicament for treatment of Syk receptor related diseases.

5-HETEROARYL SUBSTITUTED INDAZOLE-3-CARBOXAMIDES AND PREPARATION AND USE THEREOF

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Paragraph 0708; 0709, (2019/09/06)

Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of an indazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., tendinopathy, dermatitis, psoriasis, morphea, ichthyosis, Raynaud's syndrome, Darier's disease, scleroderma, cancer, abnormal cellular proliferation, angiogenesis, Alzheimer's disease, lung disease, and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as neurological conditions/disorders/diseases linked to overexpression of DYRK1A.

5-SUBSTITUTED INDAZOLE-3-CARBOXAMIDES AND PREPARATION AND USE THEREOF

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Paragraph 1365; 1366, (2015/11/09)

Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of an indazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis, Alzheimer's disease, lung disease, fibrotic disorders, cartilage (chondral) defects, and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, and neurological conditions/disorders/diseases linked to overexpression of DYRK1A.

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