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4-(4-aminobenzyl)-1LAMBDA6,4-thiazinane-1,1-dione, commonly known as amiodarone, is a medication that belongs to the class of antiarrhythmics. It is used to treat and prevent life-threatening ventricular arrhythmias by stabilizing the heart's electrical activity and reducing abnormal rhythms. Amiodarone is typically administered orally or intravenously and has a long half-life, allowing for once-daily dosing. However, it is also known for its potential for serious side effects, including lung, liver, and thyroid toxicity, which necessitates close monitoring and regular follow-up with healthcare providers.

263339-24-8

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263339-24-8 Usage

Uses

Used in Cardiology:
4-(4-aminobenzyl)-1LAMBDA6,4-thiazinane-1,1-dione is used as an antiarrhythmic medication for the treatment and prevention of serious, life-threatening ventricular arrhythmias. It works by stabilizing the heart's electrical activity and reducing abnormal rhythms, making it an important medication for managing specific heart rhythm disorders.
Used in Pharmaceutical Industry:
4-(4-aminobenzyl)-1LAMBDA6,4-thiazinane-1,1-dione is used as a key ingredient in the formulation of antiarrhythmic drugs. Its ability to stabilize the heart's electrical activity and reduce abnormal rhythms makes it a valuable component in the development of medications for the treatment and prevention of life-threatening ventricular arrhythmias.

Check Digit Verification of cas no

The CAS Registry Mumber 263339-24-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,3,3 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 263339-24:
(8*2)+(7*6)+(6*3)+(5*3)+(4*3)+(3*9)+(2*2)+(1*4)=138
138 % 10 = 8
So 263339-24-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2O2S/c12-11-3-1-10(2-4-11)9-13-5-7-16(14,15)8-6-13/h1-4H,5-9,12H2

263339-24-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(1,1-dioxo-1,4-thiazinan-4-yl)methyl]aniline

1.2 Other means of identification

Product number -
Other names 4-(1,1-dioxo-thiomorpholin-4-yl-methyl)-aniline

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:263339-24-8 SDS

263339-24-8Relevant academic research and scientific papers

NON-ATP/CATALYTIC SITE P38 MITOGEN ACTIVATED PROTEIN KINASE INHIBITORS

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Paragraph 00282, (2021/09/17)

Compounds that inhibit p38a MAPK protein, and methods of using the same, are provided for treating or preventing diseases such as cancer or inflammatory diseases.

NON-ATP/CATALYTIC SITE p38 MITOGEN ACTIVATED PROTEIN KINASE INHIBITORS

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Paragraph 00277, (2020/07/04)

Compounds that inhibit p38α MAPK protein, and methods of using the same, are provided for treating or preventing diseases such as cancer or inflammatory diseases.

Substituted indolines which inhibit receptor tyrosine kinases

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Page column 48, (2008/06/13)

Indolinones of the formula having an inhibitory effect on receptor tyrosine kinases and cyclin/CDK complexes, as well as on the proliferation of endothelial cells and various tumor cells. Exemplary are: (a) 3-Z-[1-(4-(piperidin-1-yl-methyl)-anilino)-1-phenyl-methylene]-6-ethoxycarbonyl-2-indolinone, (b) 3-Z-[(1-(4-(piperidin-1-yl-methyl)-anilino)-1-phenyl-methylene]-6-carbamoyl-2-indolinone, and (c) 3-Z-[1-(4-(piperidin-1-yl-methyl)-anilino)-1-phenyl-methylene]-6-metboxycarbonyl-2-indolinone.

Substituted indolinones with kinase inhibitory activity

-

, (2008/06/13)

Substituted indolinones of general formula having effect on various kinases and cycline/CDK complexes and on the proliferation of various tumour cells. Exemplary compounds are: 3-Z-[1-(4-(N-Benzyl-N-methyl-aminomethyl)-phenylamino)-1-methyl-methylene]-5-a

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