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(6-bromo-1,3-benzodioxol-5-yl)(3,4-dihydroquinolin-1(2H)-yl)methanone is a complex organic molecule that features a benzodioxol ring, a dihydroquinolin ring, and a methanone functional group. (6-bromo-1,3-benzodioxol-5-yl)(3,4-dihydroquinolin-1(2H)-yl)methanone is recognized for its potential as a medicinal compound in pharmaceutical research and drug development. Its unique structure and functional groups contribute to its value as a building block for synthesizing new drugs with specific pharmacological properties, making it a significant target for study and exploration in medicinal chemistry.
Used in Pharmaceutical Research and Drug Development:
(6-bromo-1,3-benzodioxol-5-yl)(3,4-dihydroquinolin-1(2H)-yl)methanone is used as a medicinal compound for its potential in pharmaceutical research and drug development. Its unique molecular structure and functional groups enable the synthesis of new drugs with desired pharmacological properties, contributing to the advancement of medicinal chemistry.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6-bromo-1,3-benzodioxol-5-yl)(3,4-dihydroquinolin-1(2H)-yl)methanone is used as a valuable building block for synthesizing new drugs. Its specific molecular properties and potential applications make it an important target for further study and exploration, with the aim of developing innovative therapeutic agents.

65367-72-8

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65367-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65367-72-8 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 65367-72:
(7*6)+(6*5)+(5*3)+(4*6)+(3*7)+(2*7)+(1*2)=148
148 % 10 = 8
So 65367-72-8 is a valid CAS Registry Number.

65367-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-bromo-1,3-benzodioxol-5-yl)-(3,4-dihydro-2H-quinolin-1-yl)methanone

1.2 Other means of identification

Product number -
Other names 1-(6-bromo-benzo[1,3]dioxole-5-carbonyl)-1,2,3,4-tetrahydro-quinoline

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:65367-72-8 SDS

65367-72-8Downstream Products

65367-72-8Relevant 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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