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3749-21-1

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3749-21-1 Usage

Description

4-Bromo-isoquinoline 2-oxide is a chemical compound with the molecular formula C9H6BrNO, belonging to the isoquinoline family. It is recognized for its capacity to engage in oxidation reactions and is a significant player in the realm of organic chemistry. 4-BROMO-ISOQUINOLINE 2-OXIDE is also being explored for its potential as a pharmaceutical intermediate and in photochemical and medicinal applications, making it a versatile and promising substance for the development of new drugs and materials.

Uses

Used in Pharmaceutical Industry:
4-Bromo-isoquinoline 2-oxide is used as a pharmaceutical intermediate for its ability to be a key component in the synthesis of various organic compounds. Its role in the development of new drugs is significant due to its reactivity and potential to be modified for specific therapeutic applications.
Used in Organic Synthesis:
In the field of organic chemistry, 4-bromo-isoquinoline 2-oxide is utilized as a building block for the creation of complex organic molecules. Its unique structure and reactivity make it a valuable asset in the synthesis of a wide range of compounds.
Used in Photochemical Applications:
4-Bromo-isoquinoline 2-oxide is also being investigated for its potential use in photochemical processes. Its ability to participate in oxidation reactions under certain conditions makes it a candidate for applications that involve light-induced chemical transformations.
Used in Medicinal Applications:
4-BROMO-ISOQUINOLINE 2-OXIDE has been studied for its potential in medicinal applications, where it could contribute to the development of new treatments and therapies. Its exploration in this area is ongoing, with the aim of leveraging its chemical properties to address various medical needs.

Check Digit Verification of cas no

The CAS Registry Mumber 3749-21-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,4 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3749-21:
(6*3)+(5*7)+(4*4)+(3*9)+(2*2)+(1*1)=101
101 % 10 = 1
So 3749-21-1 is a valid CAS Registry Number.

3749-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-2-oxidoisoquinolin-2-ium

1.2 Other means of identification

Product number -
Other names Isoquinoline,4-bromo-,2-oxide

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:3749-21-1 SDS

3749-21-1Relevant articles and documents

Electrochemical-Oxidation-Promoted Direct N-ortho-Selective Difluoromethylation of Heterocyclic N-Oxides

Zhang, Dong,Cai, Jinlin,Du, Jinze,Wang, Qingdong,Yang, Jinming,Geng, Rongqing,Fang, Zheng,Guo, Kai

supporting information, p. 1434 - 1438 (2022/03/01)

An efficient and green electrochemical N-ortho-selective difluoromethylation method of various quinoline and isoquinoline N-oxides has been developed. In this method, sodium difluoromethanesulfinate (HCF2SO2Na) was used as the source of the difluoromethyl moiety, and various N-ortho-selective difluoromethylation quinoline and isoquinoline N-oxides were obtained in good to excellent yields under a constant current. In addition, the reaction was easy to scale up and maintained a good yield. Preliminary mechanism studies suggested that the reaction undergoes a free-radical addition and hydrogen elimination pathway.

SUBSTITUTED ARYLMETHYLUREAS AND HETEROARYLMETHYLUREAS, ANALOGUES THEREOF, AND METHODS USING SAME

-

Page/Page column 241; 242, (2020/07/07)

The present invention includes substituted arylmethyl ureas and heteroarylmethyl-ureas, and compositions comprising the same, that can be used to treat or prevent hepatitis B virus (HBV) infections in a patient.

An organocatalytic enantioselective direct α-heteroarylation of aldehydes with isoquinoline: N -oxides

Bertuzzi, Giulio,Pecorari, Daniel,Bernardi, Luca,Fochi, Mariafrancesca

supporting information, p. 3977 - 3980 (2018/04/23)

A new protocol for the enantioselective direct α-heteroarylation of aldehydes with isoquinoline N-oxides, via chiral enamine catalysis, has been successfully developed. High enantiomeric excesses and moderate to good yields were achieved for a variety of α-heteroarylated aldehydes.

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