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1H-Indole, 4-bromo-6-methylis a chemical compound with the molecular formula C9H8BrN. It is a derivative of the heterocyclic compound indole, which is commonly found in plant-based foods and is also a component of some pharmaceuticals. 1H-Indole, 4-bromo-6-methylis characterized by the presence of a bromine atom at the 4th position and a methyl group at the 6th position on the indole ring. It appears as a pale yellow to light brown solid at room temperature and is known for its potential applications in various fields.

885520-48-9

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885520-48-9 Usage

Uses

Used in Pharmaceutical Industry:
1H-Indole, 4-bromo-6-methylis used as an intermediate in the synthesis of various organic compounds for pharmaceutical applications. Its unique structure and properties make it a valuable building block for the development of new drugs and medicinal agents.
Used in Agrochemical Industry:
In the agrochemical industry, 1H-Indole, 4-bromo-6-methylis utilized in the synthesis of various agrochemicals, including pesticides and herbicides. Its chemical properties allow it to be incorporated into compounds that can effectively control pests and weeds in agricultural settings.
Used in Research and Development:
1H-Indole, 4-bromo-6-methylis also used in research and development for its potential applications in medicinal chemistry and drug discovery. Its biological activity and unique structural features make it an interesting candidate for further study and exploration in the development of novel therapeutic agents.
Used in Organic Synthesis:
As a chemical compound with a distinct structure, 1H-Indole, 4-bromo-6-methylis employed in organic synthesis for the preparation of various organic compounds. Its reactivity and functional groups enable it to participate in a wide range of chemical reactions, contributing to the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 885520-48-9 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, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 885520-48:
(8*8)+(7*8)+(6*5)+(5*5)+(4*2)+(3*0)+(2*4)+(1*8)=199
199 % 10 = 9
So 885520-48-9 is a valid CAS Registry Number.

885520-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromo-6-methyl-1H-indole

1.2 Other means of identification

Product number -
Other names 4-Bromo-6-methyl indole

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:885520-48-9 SDS

885520-48-9Relevant academic research and scientific papers

CARBOXY SUBSTITUTED (HETERO) AROMATIC RING DERIVATIVES AND PREPARATION METHOD AND USES THEREOF

-

, (2017/03/21)

Carboxy-substituted (hetero)aryl derivatives, pharmaceutical compositions comprising these compounds, and methods of preparing such compounds and compositions are provided. The compounds or compositions are useful in inhibiting xanthine oxidase and urate anion transporter 1, and also can be used in the treatment or prevention of diseases associated with high blood uric acid level in mammals, especially humans.

QUINUCLIDINES FOR MODULATING ALPHA 7 ACTIVITY

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Paragraph 0251, (2016/02/29)

Provided are substituted quinuclidine compounds, pharmaceutical compositions comprising such compounds, and methods of modulating α7 nicotinic acetylcholine receptors and treating neurological disorders using such compounds.

Continuous-flow synthesis of monoarylated acetaldehydes using aryldiazonium salts

Chernyak, Natalia,Buchwald, Stephen L.

, p. 12466 - 12469 (2012/09/05)

Anilines and ethyl vinyl ether can be used as precursors for a process that is the synthetic equivalent of the α-arylation of acetaldehyde enolate. The reaction manifests a high level of functional group compatibility, allowing the ready preparation of a number of synthetically valuable compounds.

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