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7-bromo-4-methyl-1H-indole is a heterocyclic aromatic organic compound with the molecular formula C9H8BrN. It is an indole derivative, which is commonly used as a building block in organic synthesis, particularly in the pharmaceutical industry for the production of various drugs. This chemical has been reported to possess a range of biological activities, including antifungal, antimicrobial, and anticancer properties. Furthermore, it has been studied for its potential use as a fluorescent dye and as a ligand for metal catalysis. Due to its potential health and environmental hazards, it is crucial to handle this chemical with caution and follow appropriate safety protocols.

165669-07-8

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165669-07-8 Usage

Uses

Used in Pharmaceutical Industry:
7-bromo-4-methyl-1H-indole is used as a building block in organic synthesis for the production of various drugs. Its unique chemical structure and biological activities make it a valuable component in the development of new pharmaceutical compounds.
Used in Antifungal Applications:
7-bromo-4-methyl-1H-indole is used as an antifungal agent due to its ability to inhibit the growth of various fungi. Its incorporation into pharmaceutical formulations can help combat fungal infections and improve treatment outcomes.
Used in Antimicrobial Applications:
This chemical is used as an antimicrobial agent, demonstrating its effectiveness against a range of microorganisms. Its incorporation into antimicrobial products can help prevent the spread of infections and promote overall health.
Used in Anticancer Applications:
7-bromo-4-methyl-1H-indole is used as an anticancer agent, exhibiting potential inhibitory effects on tumor growth and progression. Its unique properties make it a promising candidate for further research and development in cancer treatment.
Used in Fluorescent Dye Applications:
This chemical has been studied for its potential use as a fluorescent dye, which can be utilized in various scientific and industrial applications, such as imaging, diagnostics, and sensing.
Used in Metal Catalysis Applications:
7-bromo-4-methyl-1H-indole is used as a ligand for metal catalysis, enhancing the efficiency and selectivity of various chemical reactions. Its unique properties make it a valuable component in the development of new catalytic systems.

Check Digit Verification of cas no

The CAS Registry Mumber 165669-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,6,6 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 165669-07:
(8*1)+(7*6)+(6*5)+(5*6)+(4*6)+(3*9)+(2*0)+(1*7)=168
168 % 10 = 8
So 165669-07-8 is a valid CAS Registry Number.

165669-07-8SDS

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 7-Bromo-4-methyl-1H-indole

1.2 Other means of identification

Product number -
Other names 7-Bromo-4-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:165669-07-8 SDS

165669-07-8Relevant academic research and scientific papers

Aromatic ring liquid crystal compound and liquid crystal composition and application thereof

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Paragraph 0116-0118; 0127-0128; 0147-0149; 0156-0157, (2021/05/29)

The invention relates to an aromatic ring liquid crystal compound, a liquid crystal composition and an assembly suitable for a microwave region and a millimeter wave region of a high-frequency technology or an electromagnetic spectrum, and particularly a phase shifter and a microwave array antenna. The liquid crystal composition provided by the invention at least comprises a compound represented by a general formula I. The liquid crystal composition provided by the invention is good in stability, high in response speed and wide in liquid crystal phase temperature range.

IRAK DEGRADERS AND USES THEREOF

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Paragraph 2467; 2468, (2019/07/10)

The present invention provides compounds, compositions thereof, and methods of using the same.

HETEROCYCLIC DERIVATIVES AS RORGAMMA MODULATORS

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Page/Page column 63, (2016/07/27)

The present invention provides novel compounds of formula (I) that are modulators of RORgamma. These compounds, and pharmaceutical compositions comprising the same, are suitable means for treating any disease wherein the modulation of RORgamma has therapeutic effects, for instance in autoimmune diseases, autoimmune-related diseases, inflammatory diseases, fibrotic diseases, or cholestatic diseases.

Integrin expression inhibitors

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, (2008/06/13)

The present invention provides an integrin expression inhibitor, and an agent for treating arterial sclerosis, psoriasis, cancer, retinal angiogenesis, diabetic retinopathy or inflammatory diseases, an anticoagulant, or a cancer metastasis suppressor on the basis of an integrin inhibitory action. Namely, it provides an integrin expression inhibitor comprising, as an active ingredient, a sulfonamide compound represented by the following formula (I), a pharmacologically acceptable salt thereof or a hydrate of them. In the formula, B means a C6-C10 aryl ring or 6- to 10-membered heteroaryl ring which may have a substituent and in which a part of the ring may be saturated; K means a single bond, —CH═CH— or —(CR4bR5b)mb— (wherein R4b and R5b are the same as or different from each other and each means hydrogen atom or a C1-C4 alkyl group; and mb means an integer of 1 or 2); R1 means hydrogen atom or a C1-C6 alkyl group; Z means a single bond or —CO—NH—; and R means a C6-C10 aryl ring or 6- to 10-membered heteroaryl ring which may have a substituent and in which a part of the ring may be saturated, respectively.

INTEGRIN EXPRESSION INHIBITORS

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, (2008/06/13)

The present invention provides an integrin expression inhibitor, and an agent for treating arterial sclerosis, psoriasis, cancer, retinal angiogenesis, diabetic retinopathy or inflammatory diseases, an anticoagulant, or a cancer metastasis suppressor on the basis of an integrin inhibitory action. Namely, it provides an integrin expression inhibitor comprising, as an active ingredient, a sulfonamide compound represented by the following formula (I), a pharmacologically acceptable salt thereof or a hydrate of them. In the formula, B means a C6-C10 aryl ring or 6- to 10-membered heteroaryl ring which may have a substituent and in which a part of the ring may be saturated; K means a single bond, -CH=CH- or - (CR4bR5b)mb- (wherein R4b and R5b are the same as or different from each other and each means hydrogen atom or a C1-C4 alkyl group; and mb means an integer of 1 or 2); R1 means hydrogen atom or a C1-C6 alkyl group; Z means a single bond or -CO-NH-; and R means a C6-C10 aryl ring or 6- to 10-membered heteroaryl ring which may have a substituent and in which a part of the ring may be saturated, respectively.

Sulfonamide-containing indole compounds

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, (2008/06/13)

The present invention creates a novel antiangiogenic agent and provides an antitumor agent which shows high safety as compared with conventional antitumor agents, has a sure effect and is able to be administered for a long period. That is, it provides an indole compound represented by the following formula (I), its pharmacologically acceptable salt or hydrates thereof. In the formula, R1 represents hydrogen atom, a halogen atom or cyano group; R2 and R3 are the same as or different from and each represents hydrogen atom, a C1-C4 lower alkyl group or a halogen atom; R4 represents hydrogen atom or a C1-C4 lower alkyl group; and the ring A represents cyanophenyl group, aminosulfonylphenyl group, aminopyridyl group, aminopyrimidyl group, a halopyridyl group or cyanothiophenyl group, provided that the case where all of R1, R2 and R3 are hydrogen atoms, where both R2 and R3 are hydrogen atoms or where the ring A is aminosulfonyl group and both R1 and R2 are halogen atoms is excluded. Further, when the ring A is cyanophenyl group, 2-amino-5-pyridyl group or a 2-halo-5-pyridyl group and R1 is cyano group or a halogen atom, at least one of R2 and R3 should not be a hydrogen atom.

A focused compound library of novel N-(7-indolyl)benzenesulfonamides for the discovery of potent cell cycle inhibitors

Owa, Takashi,Okauchi, Tatsuo,Yoshimatsu, Kentaro,Sugi, Naoko Hata,Ozawa, Yoichi,Nagasu, Takeshi,Koyanagi, Nozomu,Okabe, Tadashi,Kitoh, Kyosuke,Yoshino, Hiroshi

, p. 1223 - 1226 (2007/10/03)

A series of compounds containing an N-(7-indolyl)benzenesulfonamide pharmacophore was synthesized and evaluated as a potential antitumor agent. Cell cycle analysis with P388 murine leukemia cells revealed that there were two different classes of potent cell cycle inhibitors; one disrupted mitosis and the other caused G1 accumulation. Herein described is the SAR summary of the substituent patterns on this pharmacophore template. (C) 2000 Elsevier Science Ltd. All rights reserved.

Heterobicyclic sulfonamide and sulfonic ester derivatives

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, (2008/06/13)

Novel heterobicyclic sulfonamide and sulfonic ester derivatives represented by the following general formula(I), which exhibit an antitumor activity and are lowly toxic, and processes for the preparation thereof. A sulfonamide derivative and a sulfonic ester derivative represented by the general formula (I) or a pharmacologically acceptable salt thereof: STR1 wherein A represents a monocyclic or bicyclic aromatic ring which may be substituted; B represents a six-membered unsaturated hydrocarbon ring or a six-membered unsaturated heterocycle containing one nitrogen atom, each of which may be substituted; C represents a five-membered heterocycle containing one or two nitrogen atoms which may be substituted; W represents a single bond or a group represented by formula --CH=CH--; X represents a group represented by formula --N(R1)-- or oxygen; Y represents carbon or nitrogen; Z represents a group represented by formula --N(R2)-- or nitrogen; and R1 and R2 may be the same or different from each other and each represent hydrogen or lower alkyl.

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