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4-(CHLOROACETYL)-3,4-DIHYDRO-2H-1,4-BENZOTHIAZINE, with the Chemical Abstracts Service number 60028-69-3, is an organic compound characterized by the molecular formula C10H10ClNO2S. It is a benzothiazine derivative featuring a chloroacetyl group. This white to off-white solid is sparingly soluble in water but soluble in organic solvents like ethanol and dichloromethane. It plays a significant role as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and is utilized as a building block in medicinal chemistry for the development of new drugs and therapeutic agents.

20751-75-1

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20751-75-1 Usage

Uses

Used in Pharmaceutical Industry:
4-(CHLOROACETYL)-3,4-DIHYDRO-2H-1,4-BENZOTHIAZINE is used as a key intermediate in the synthesis of various pharmaceuticals for its potential to contribute to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical field, 4-(CHLOROACETYL)-3,4-DIHYDRO-2H-1,4-BENZOTHIAZINE is utilized as an intermediate in the creation of agrochemicals, highlighting its importance in developing compounds for agricultural applications.
Used in Medicinal Chemistry Research:
4-(CHLOROACETYL)-3,4-DIHYDRO-2H-1,4-BENZOTHIAZINE is employed as a building block in medicinal chemistry, where it aids in the study and development of chemical compounds for diverse applications within the pharmaceutical and agricultural industries.

Check Digit Verification of cas no

The CAS Registry Mumber 20751-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,5 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20751-75:
(7*2)+(6*0)+(5*7)+(4*5)+(3*1)+(2*7)+(1*5)=91
91 % 10 = 1
So 20751-75-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H10ClNOS/c11-7-10(13)12-5-6-14-9-4-2-1-3-8(9)12/h1-4H,5-7H2

20751-75-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H61095)  4-(2-Chloroacetyl)-2H-1,4-benzothiazine, 97%   

  • 20751-75-1

  • 250mg

  • 505.0CNY

  • Detail
  • Alfa Aesar

  • (H61095)  4-(2-Chloroacetyl)-2H-1,4-benzothiazine, 97%   

  • 20751-75-1

  • 1g

  • 1617.0CNY

  • Detail

20751-75-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-(2,3-dihydro-1,4-benzothiazin-4-yl)ethanone

1.2 Other means of identification

Product number -
Other names 4-(chloroacetyl)-3,4-dihydro-2H-1,4-benzothiazine

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:20751-75-1 SDS

20751-75-1Downstream Products

20751-75-1Relevant academic research and scientific papers

Indoline and piperazine containing derivatives as a novel class of mixed D2/D4 receptor antagonists. Part 1: Identification and structure-activity relationships

Zhao, He,Thurkauf, Andrew,He, Xiaoshu,Hodgetts, Kevin,Zhang, Xiaoyan,Rachwal, Stanislaw,Kover, Renata X.,Hutchison, Alan,Peterson, John,Kieltyka, Andrzej,Brodbeck, Robbin,Primus, Renee,Wasley, Jan W.F.

, p. 3105 - 3109 (2007/10/03)

Optimization of the lead compound 2-[-4-(4-chloro-benzyl)-piperazin-1-yl]-1-(2,3-dihydro-indol-1-yl)-ethanone 1 by systematic structure-activity relation (SAR) studies lead to two potent compounds 2-[-4-(4-chloro-benzyl)-piperazin-1-yl]-1-(2-methy-2,3-dihydro-indol-1-yl)- ethanone 2n and 2-[-4-(4-chloro-benzyl)-piperazin-1-yl]-1-(2-methy-2,3-dihydro-indol-1-yl)- ethanone 7b. Their related synthesis was also reported.

1,2-Dihydro-1-oxopyrrolophenothiazine-2-carboxamides and Congeners, Dual Cyclooxygenase/5-Lipoxygenase Inhibitors with Antiinflammatory Activity

Mylari, Banavara L.,Carty, Thomas J.,Moore, Peter F.,Zembrowski, William J.

, p. 2019 - 2024 (2007/10/02)

A series of 1,2-dihydro-1-oxopyrrolophenothiazine, 1,2-dihydro-1-oxopyrrolophenoxazine, and 1,2-dihydro-1-oxopyrroloacridine-2-carboxamides were prepared by reaction of 1,2-dihydro-1-oxopyrrolophenothiazine or other

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