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6,11-Dihydro-6-methyl-dibenzo[c,f][1,2]thiazepin-11-ol 5,5-Dioxide is a white solid compound that serves as a crucial reagent in the synthesis of Dibenzo[c,f][1,2]thiazepine derivatives. Its unique chemical structure and properties make it a valuable component in various chemical reactions and applications.

26638-56-2

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26638-56-2 Usage

Uses

Used in Pharmaceutical Industry:
6,11-Dihydro-6-methyl-dibenzo[c,f][1,2]thiazepin-11-ol 5,5-Dioxide is used as a reagent for the synthesis of Dibenzo[c,f][1,2]thiazepine derivatives, which are known for their potential therapeutic applications. These derivatives have been studied for their potential use in the development of new drugs and pharmaceutical compounds.
Used in Chemical Research:
6,11-Dihydro-6-methyl-dibenzo[c,f][1,2]thiazepin-11-ol 5,5-Dioxide is also used as a reagent in various chemical research applications. Its unique properties and structure make it a valuable tool for studying chemical reactions and developing new synthetic methods.
Used in Organic Synthesis:
6,11-Dihydro-6-methyl-dibenzo[c,f][1,2]thiazepin-11-ol 5,5-Dioxide is employed as a reagent in organic synthesis, where it can be used to create a variety of complex organic compounds. Its versatility and stability make it a popular choice for chemists working in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 26638-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,3 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26638-56:
(7*2)+(6*6)+(5*6)+(4*3)+(3*8)+(2*5)+(1*6)=132
132 % 10 = 2
So 26638-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO3S/c1-15-12-8-4-2-6-10(12)14(16)11-7-3-5-9-13(11)19(15,17)18/h2-9,14,16H,1H3

26638-56-2SDS

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

1.2 Other means of identification

Product number -
Other names 5,11-Dihydro-10,10-dioxo-5-hydroxy-11-methyl-dibenzo-<c,f>-thiazepin

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:26638-56-2 SDS

26638-56-2Relevant academic research and scientific papers

Design, synthesis and biological evaluation of substituted dioxodibenzothiazepines and dibenzocycloheptanes as farnesyltransferase inhibitors

Gilleron, Pauline,Wlodarczyk, Nicolas,Houssin, Raymond,Farce, Amaury,Laconde, Guillaume,Goossens, Jean-Francois,Lemoine, Amelie,Pommery, Nicole,Henichart, Jean-Pierre,Millet, Regis

, p. 5465 - 5471 (2008/03/11)

A new series of FTase inhibitors containing a tricyclic moiety-dioxodibenzothiazepine or dibenzocycloheptane-has been designed and synthesized. Among them, dioxodibenzothiazepine 18d displayed significant inhibitory FTase activity (IC50 = 17.3

Synthesis and anticonvulsant activity of new dibenzo[1,2]thiazepine S,S-dioxides

Diaz,Montero,Vega,Darias,Tello,Abdallah

, p. 157 - 161 (2007/10/02)

A new series of 11-substituted 6,11-dihydro-6-methyl-dibenzo[c,f][l,2]thiazepine S,S-dioxides was synthesized. Some of the components show significant anticonvulsant activity in the MES, pentetrazol and strychnine tests. The more active compounds are devoid of neurotoxic effects.

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