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Dibenzo[b,f][1,4]thiazepin-11-amine is a chemical compound belonging to the class of dibenzothiazepines, which are tricyclic heterocycles with a sulfur atom. It is characterized by its unique molecular structure and potential applications in various fields, particularly in the synthesis of other complex molecules with potential biological activities.

5786-26-5

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5786-26-5 Usage

Uses

Used in Pharmaceutical Industry:
Dibenzo[b,f][1,4]thiazepin-11-amine is used as a reagent for the preparation of other triand tetracyclic heterocycles that have potential central nervous system (CNS) activity. These synthesized compounds may exhibit therapeutic effects on various neurological disorders and conditions, making them valuable in the development of novel pharmaceuticals.
Used in Organic Synthesis:
Dibenzo[b,f][1,4]thiazepin-11-amine is also used as a reactant to synthesize 2-substituted-3-cyano-4-imino-4-H-dibenzo[b,f][1,3]diazino[2,1-d][1,4]thiazepines. These compounds may have anticancer properties, and their synthesis contributes to the ongoing research and development of new cancer treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 5786-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,8 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5786-26:
(6*5)+(5*7)+(4*8)+(3*6)+(2*2)+(1*6)=125
125 % 10 = 5
So 5786-26-5 is a valid CAS Registry Number.

5786-26-5SDS

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 11-aminodibenzo<b,f><1,4>thiazepine

1.2 Other means of identification

Product number -
Other names Dibenzo[b,f][1,4]thiazepin-11-amine

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:5786-26-5 SDS

5786-26-5Relevant academic research and scientific papers

Three-Component Synthesis of Dibenzoxazepinamines and Dibenzothiazepinamines under Transition-Metal-Free Conditions

Chen, Shanping,Deng, Guo-Jun,Fang, Fang,Jiang, Shuxin,Lei, Hanwen

, p. 15658 - 15664 (2021/11/12)

A convenient and efficient strategy for the synthesis of dibenzoxazepinamines and dibenzothiazepinamines has been developed. This three-component approach started from 2-nitrobenzaldehydes, 2-aminophenols, and methoxyammonium chlorides under metal-free conditions. The protocol has the advantages of readily available starting materials, simple and facile conditions, gram-scale synthesis, and broad substrate scope, providing an efficient and practical strategy for the preparation of potential drug-active dibenzoxazepinamines and dibenzothiazepinamines in one pot.

Base-promoted synthesis of dibenzoxazepinamines and quinazolinimines under metal-free conditions

Feng, Jian-Bo,Wu, Xiao-Feng

supporting information, p. 4522 - 4526 (2015/09/15)

An interesting base-promoted protocol for the synthesis of dibenzo[b,f][1,4]oxazepin-11-amines and quinazolinimines has been developed. Started from commercially available 2-fluorobenzonitriles, 2-aminophenols and 2-aminoethanol, good to excellent yields

A PROCESS FOR THE PREPARATION OF QUETIAPINE

-

Page/Page column 9, (2009/09/05)

The invention relates to a method for the preparation of 11- (4- [2- (2- hydroxyethoxy) ethyl] -1-piperazinyl] dibenzo [b, f ] -1, 4-thiazepine and pharmaceutically acceptable salts thereof comprising the reaction of 1- [2- (hydroxyethoxy) -ethyl] piperazine with dibenzo [b, f] [1, 4] thiazepin-11-ylamine.

Synthesis of 11-Aminodibenzo[b,f][1,4]thiazepines and Fluoro Derivatives

Mettey, Yvette,Lehuede, Jacques,Vierfond, Jean-Michel

, p. 465 - 467 (2007/10/03)

The reaction of halogenobenzonitriles with 2-aminobenzenethiol is a new route, in a "one-pot" or two-step approach, to 11-aminodibenzo[b,f][1,4]thiazepine and fluoro derivatives.

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