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6-Methoxy-5-Methyl 1H-indole is a chemical compound that belongs to the class of organic compounds known as indoles. These are aromatic heterocyclic compounds characterized by the fusion of a benzene and a pyrrole ring. 6-Methoxy-5-Methyl 1H-indole is distinguished by the presence of a methoxy group on the sixth carbon atom and a methyl group on the fifth carbon atom in the indole ring. It is significant in scientific research and is utilized as a chemical reagent, with potential biological activities that are yet to be fully explored and established.

1071973-95-9

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1071973-95-9 Usage

Uses

Used in Scientific Research:
6-Methoxy-5-Methyl 1H-indole is used as a chemical reagent in various scientific research applications. Its unique structure and properties make it a valuable compound for studying the chemistry and biology of indole derivatives.
Used in Pharmaceutical Development:
As an indole derivative, 6-Methoxy-5-Methyl 1H-indole may possess potential biological activities that could be harnessed in the development of pharmaceuticals. Although specific activities have not been definitively established, its exploration in drug discovery could lead to the identification of new therapeutic agents.
Used in Chemical Synthesis:
6-Methoxy-5-Methyl 1H-indole's structure and functional groups make it a candidate for use in chemical synthesis processes. It can potentially serve as an intermediate or building block in the synthesis of more complex organic molecules with specific applications in various industries.
Used in Material Science:
The properties of 6-Methoxy-5-Methyl 1H-indole, such as solubility, melting point, and boiling point, may be exploited in material science for the development of new materials with tailored characteristics, depending on its purity and other factors.

Check Digit Verification of cas no

The CAS Registry Mumber 1071973-95-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,1,9,7 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1071973-95:
(9*1)+(8*0)+(7*7)+(6*1)+(5*9)+(4*7)+(3*3)+(2*9)+(1*5)=169
169 % 10 = 9
So 1071973-95-9 is a valid CAS Registry Number.

1071973-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Methoxy-5-methyl-1H-indole

1.2 Other means of identification

Product number -
Other names 6-Methoxy-5-methylindole

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:1071973-95-9 SDS

1071973-95-9Downstream Products

1071973-95-9Relevant academic research and scientific papers

(AZA)INDOLE DERIVATIVE AND USE THEREOF FOR MEDICAL PURPOSES

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Page/Page column 26, (2009/12/27)

The present invention provides compounds useful as agents for the prevention or treatment of a disease associated with abnormal serum uric acid level which has a uricosuric activity or the like. The present invention relates to (aza)indole derivatives represented by the following general formula (I) having xanthine oxidase inhibitory activities and useful as agents for the prevention or treatment of a disease associated with abnormality of serum uric acid level, prodrugs thereof, or salts thereof. In the formula (I), T represents nitro or cyano and the like; ring J represents aryl or heteroaryl and the like; Q represents carboxy or 5-tetazolyl and the like; Y represents H, OH, NH2, halogen, nitro, alkyl, alkoxy and the like; X1, X2 and X3 independently represent CR2 or N; R1 and R2 independently represent halogen, cyano, haloalkyl, A-D-E-G, -N(-D-E-G)2 and the like, in the formula, A represents a single bond, O, S and the like; D and G independently represent optionally substituted alkylene, cycloalkylene, heterocycloalkylene, arylene, heteroarylene and the like; E represents a single bond, O, S, COO, SO2 and the like.

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