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(2-bromo-4,5-dimethoxyphenyl)(2,3-dihydro-1H-indol-1-yl)methanone is a synthetic chemical compound that features a 2-bromo-4,5-dimethoxyphenyl group and a 2,3-dihydro-1H-indol-1-yl group connected to a methanone functional group. (2-bromo-4,5-dimethoxyphenyl)(2,3-dihydro-1H-indol-1-yl)methanone is primarily utilized in laboratory research due to its potential pharmacological properties and is being investigated for its possible applications in the development of new drug candidates for various medical conditions.

65367-71-7

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65367-71-7 Usage

Uses

Used in Pharmaceutical Research:
(2-bromo-4,5-dimethoxyphenyl)(2,3-dihydro-1H-indol-1-yl)methanone is used as a research compound for exploring its potential as a new drug candidate. Its unique structure and properties make it a promising candidate for the development of medications targeting a range of medical conditions.
Used in Laboratory Research:
In a controlled laboratory setting, (2-bromo-4,5-dimethoxyphenyl)(2,3-dihydro-1H-indol-1-yl)methanone is used as a test subject to study its pharmacological properties and potential interactions with biological systems. This research is crucial for understanding its safety, efficacy, and possible therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 65367-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,6 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65367-71:
(7*6)+(6*5)+(5*3)+(4*6)+(3*7)+(2*7)+(1*1)=147
147 % 10 = 7
So 65367-71-7 is a valid CAS Registry Number.

65367-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-bromo-4,5-dimethoxyphenyl)-(2,3-dihydroindol-1-yl)methanone

1.2 Other means of identification

Product number -
Other names 6-bromo-3-methoxy-N-tetrahydroquinolyl-benzamide

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:65367-71-7 SDS

65367-71-7Downstream Products

65367-71-7Relevant academic research and scientific papers

Intramolecular direct dehydrohalide coupling promoted by KOtBu: Total synthesis of amaryllidaceae alkaloids anhydrolycorinone and oxoassoanine

De, Subhadip,Ghosh, Santanu,Bhunia, Subhajit,Sheikh, Javeed Ahmad,Bisai, Alakesh

, p. 4466 - 4469 (2012/10/29)

A transition-metal-free intramolecular dehydrohalide coupling via intramolecular homolytic aromatic substitution (HAS) with aryl radicals has been developed in the presence of potassium tert-butoxide and an organic molecule as the catalyst. The methodology has been applied to a concise synthesis of Amaryllidaceae alkaloids viz. oxoassoanine (1b), anhydrolycorinone (1d), and other related structures. Interestingly, the method also works only in the presence of potassium tert-butoxide.

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