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26723-60-4

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  • 3-Chloro-6,11-dihydro-6-methyldibenzo[c,f][1,2]thiazepin-11-ol 5,5-dioxide Manufacturer/High quality/Best price/In stock

    Cas No: 26723-60-4

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  • High quality 5,8-Dichloro-10-Dioxo-11-Methyl-Dibenzo[C,F] [1,2] Thiazepine supplier in China

    Cas No: 26723-60-4

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  • 3-Chloro-11-hydroxy-6-methyl-6,11-dihydrodibenzo[c,f][1,2]thiazepine 5,5-dioxide; Tianeptine Intermediate CAS:26723-60-4 from fandachem

    Cas No: 26723-60-4

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26723-60-4 Usage

Description

3-Chloro-6,11-dihydro-6-methyldibenzo[c,f][1,2]thiazepin-11-ol 5,5-dioxide is a chemical compound belonging to the dibenzothiazepine class. It is characterized by its unique molecular structure, which features a 6-membered thiazepine ring fused to two benzene rings, with a chlorine atom at the 3-position, a methyl group at the 6-position, and a hydroxyl group at the 11-position. The compound also has a 5,5-dioxide functional group, which contributes to its chemical properties and potential applications.

Uses

Used in Pharmaceutical Industry:
3-Chloro-6,11-dihydro-6-methyldibenzo[c,f][1,2]thiazepin-11-ol 5,5-dioxide is used as an intermediate in the synthesis of Dibenzo[c,f][1,2]thiazepine derivatives for the pharmaceutical industry. These derivatives are known for their diverse biological activities, including potential applications in the development of new drugs for various therapeutic areas.
Used in Chemical Synthesis:
In the field of chemical synthesis, 3-Chloro-6,11-dihydro-6-methyldibenzo[c,f][1,2]thiazepin-11-ol 5,5-dioxide serves as a key building block for the creation of more complex molecules with specific properties. Its unique structure allows for further functionalization and modification, making it a valuable starting material for the synthesis of novel compounds with potential applications in various industries, such as materials science, agrochemicals, and pharmaceuticals.
Used in Research and Development:
3-Chloro-6,11-dihydro-6-methyldibenzo[c,f][1,2]thiazepin-11-ol 5,5-dioxide is also utilized in research and development settings, where it can be employed to study the structure-activity relationships of dibenzothiazepine derivatives. This knowledge can be applied to optimize the properties of these compounds for specific applications, such as improving their pharmacological profiles or enhancing their stability and solubility.

Check Digit Verification of cas no

The CAS Registry Mumber 26723-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,7,2 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26723-60:
(7*2)+(6*6)+(5*7)+(4*2)+(3*3)+(2*6)+(1*0)=114
114 % 10 = 4
So 26723-60-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H12ClNO3S/c1-16-12-5-3-2-4-10(12)14(17)11-7-6-9(15)8-13(11)20(16,18)19/h2-8,14,17H,1H3

26723-60-4SDS

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 3-chloro-6-methyl-5,5-dioxo-11H-benzo[c][2,1]benzothiazepin-11-ol

1.2 Other means of identification

Product number -
Other names 3-chloro-6-methyldibenzo[c,f][1,2]thiazepin-11(6H)-ol S,S-dioxide

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:26723-60-4 SDS

26723-60-4Relevant articles and documents

NOVEL PROCESS FOR THE PREPARATION OF 7-((3-CHLORO-6-METHYL-5,5-DIOXO-6,11-DIHYDRODIBENZO(C,F)(1,2) THIAZEPIN-11-YL)AMINO)HEPTANOATE

-

Page/Page column 5, (2010/08/05)

The present invention relates to a novel process for the preparation of sodium 7-((3-Chloro-6-methyl-5,5-dioxo-6,11-dihydrodibenzo(c,f)(1,2)thiazepin-11-yl)amino)heptanoate and intermediates. The invention also encompasses isolation of an essentially non-hygroscopic compound which is substantially pure.

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