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702670-17-5

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702670-17-5 Usage

Description

(2,3-Dihydro-3-oxo-4H-1,4-benzothiazin-4-yl)acetic acid methyl ester, 2,3-Dihydro-4-(2-methoxy-2-oxoethyl)-3-oxo-4H-1,4-benzothiazine are benzothiazine derivatives characterized by the presence of a benzothiazine core structure, a ketone group, an ester group, and a methoxy group. These compounds are utilized in medicinal chemistry and pharmaceutical research for the development of new drugs and as synthetic building blocks for creating novel organic compounds with diverse biological activities.

Uses

Used in Pharmaceutical Research:
(2,3-Dihydro-3-oxo-4H-1,4-benzothiazin-4-yl)acetic acid methyl ester, 2,3-Dihydro-4-(2-methoxy-2-oxoethyl)-3-oxo-4H-1,4-benzothiazine is used as a pharmaceutical research compound for the development of new drugs due to its unique structural features and potential biological activities.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2,3-Dihydro-3-oxo-4H-1,4-benzothiazin-4-yl)acetic acid methyl ester, 2,3-Dihydro-4-(2-methoxy-2-oxoethyl)-3-oxo-4H-1,4-benzothiazine is used as a synthetic building block for the creation of novel organic compounds with diverse biological activities, contributing to the advancement of drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 702670-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,2,6,7 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 702670-17:
(8*7)+(7*0)+(6*2)+(5*6)+(4*7)+(3*0)+(2*1)+(1*7)=135
135 % 10 = 5
So 702670-17-5 is a valid CAS Registry Number.

702670-17-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl (3-oxo-2,3-dihydro-4H-1,4-benzothiazin-4-yl)acetate

1.2 Other means of identification

Product number -
Other names (3-Oxo-2,3-dihydro-benzo[1,4]oxazin-4-yl)-acetic acid ethyl ester

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:702670-17-5 SDS

702670-17-5Relevant articles and documents

Novel 1,4-benzothiazine derivatives: synthesis, crystal structure, and anti-bacterial properties

Sebbar, Nada Kheira,Mekhzoum, Mohamed El Mehdi,Essassi, El Mokhtar,Zerzouf, Abdelfettah,Talbaoui, Ahmed,Bakri, Youssef,Saadi, Mohamed,Ammari, Lahcen El

, p. 6845 - 6862 (2016/08/25)

In order to develop relatively small molecules as pharmacologically active molecules, novel 1,4-benzothiazine derivatives with triazole and oxazolidinone were synthesized. In this study, a series of 1,2,3-triazolylmethyl-1,4-benzothiazine derivatives were developed by exploiting a click chemistry reaction using a CuI-catalyzed Huisgen [3?+?2] cycloaddition. Starting from 2-(substituted)-3,4-dihydro-2H-1,4-benzothiazi-3-one, a number of 1,4-benzothiazine derivatives were also synthesized using different alkylating agents to give a 4-(substituted)-2-(substituted)-3,4-dihydro-2H-1,4-benzothiazi-3-one in good yields. The crystal and molecular structure of compound oxazolidin-2-one in basic benzothiazine was established by single-crystal X-ray diffraction. The newly synthesized products were subjected to in vitro biological evaluation. The result indicated that the compounds show convincing antibacterial activities against different microorganisms. All structures of the synthesized compounds were elucidated on the basis of spectral analyses and chemical reactions.

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