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1153885-37-0

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1153885-37-0 Usage

Description

5-Bromo-6-chloro-1,3-dihydro-2H-indol-2-one is an organic heterocyclic compound characterized by the molecular formula C8H6BrClNO. It features both bromine and chlorine atoms within its structure, contributing to its unique chemical properties. This white crystalline solid is utilized as a versatile building block in organic synthesis and pharmaceutical research, particularly for the development of biologically active molecules and potential new drugs and agrochemicals. Due to its potential hazards, it is crucial to handle this compound with care and adhere to proper safety protocols.

Uses

Used in Organic Synthesis:
5-Bromo-6-chloro-1,3-dihydro-2H-indol-2-one serves as a key intermediate in organic synthesis, facilitating the creation of a variety of complex organic molecules. Its presence of bromine and chlorine atoms allows for further functionalization and modification, making it a valuable component in the synthesis of advanced organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-Bromo-6-chloro-1,3-dihydro-2H-indol-2-one is used as a building block for the synthesis of biologically active molecules. Its unique structure and reactivity enable the development of new drug candidates with potential therapeutic applications.
Used in Drug Development:
5-Bromo-6-chloro-1,3-dihydro-2H-indol-2-one is employed in the development of new drugs, leveraging its chemical properties to create novel pharmaceutical agents. Its potential role in medicinal chemistry makes it a promising candidate for the treatment of various diseases and conditions.
Used in Agrochemical Development:
5-BroMo-6-chloro-1,3-dihydro-2H-indol-2-one also finds application in the development of agrochemicals, where it can be used to create new pesticides, herbicides, or other agricultural chemicals. Its ability to be modified and functionalized makes it a valuable asset in the design of effective and targeted agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1153885-37-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,3,8,8 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1153885-37:
(9*1)+(8*1)+(7*5)+(6*3)+(5*8)+(4*8)+(3*5)+(2*3)+(1*7)=170
170 % 10 = 0
So 1153885-37-0 is a valid CAS Registry Number.

1153885-37-0SDS

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 5-bromo-6-chloro-1,3-dihydroindol-2-one

1.2 Other means of identification

Product number -
Other names 5-bromo-6-chloroindolin-2-one

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:1153885-37-0 SDS

1153885-37-0Upstream product

1153885-37-0Downstream Products

1153885-37-0Relevant articles and documents

INDOLINONE COMPOUNDS FOR USE AS MAP4K1 INHIBITORS

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Page/Page column 58, (2020/05/15)

The present disclosure is directed to compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein ring A, ring C, X1, X2, L1, R1, R2, R3, R4, R5, R6, R7, m and n are as defined herein, which are useful as MAP4K1 inhibitors, processes for their preparation, pharmaceutical compositions comprising the compounds, and the use of the compounds or the compositions in the treatment or prevention of various diseases, conditions and/or disorders mediated by MAP4K1.

OLEFIN SUBSTITUTED OXINDOLES HAVING AMPK ACTIVITY

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Page/Page column 61; 62, (2015/01/07)

The present invention relates to compounds of formula (I), which have valuable pharmacological properties, in particular are activators of AMPK and which are therefore useful in the treatment of certain disorders that can be prevented or treated by activation of this receptor. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2.

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