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4H-1,4-Benzothiazine-2-carboxylic acid, 3-phenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28863-86-7

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28863-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28863-86-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,6 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28863-86:
(7*2)+(6*8)+(5*8)+(4*6)+(3*3)+(2*8)+(1*6)=157
157 % 10 = 7
So 28863-86-7 is a valid CAS Registry Number.

28863-86-7SDS

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 ethyl 3-phenyl-4H-1,4-benzothiazine-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-carbethoxy-3-phenyl-4H-<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:28863-86-7 SDS

28863-86-7Relevant academic research and scientific papers

Umpolung Strategy with 2-Aminothiophenols: Access to 2-Arylbenzothiazine Derivatives from Alkyl Aryl Ketones

Nguyen, Thanh Binh,Retailleau, Pascal

supporting information, p. 5380 - 5384 (2020/11/02)

Strong Br?nsted acids were found to catalyze the oxidative condensation of 2-aminothiophenols with aryl alkyl ketones in DMSO to provide a wide range of complex 2-arylbenzothiazines. With acetophenones, dimeric 2-arylbenzothiazines were formed. On the other hand, the reaction with propiophenones resulted in 2:1 adducts whereas 1:1 adducts were produced with isobutyrophenones, benzoylacetonitrile and ethyl benzoylacetate. (Figure presented.).

SYNTHESIS, STRUCTURE, AND CHEMISTRY OF A 1-THIA-4-AZANAPHTHALENE

Sakoda, Vianne M.,Whittle, Robert R.,Olofson, R. A.

, p. 2635 - 2638 (2007/10/02)

From a crystal structure determination and thermal rearrangement studies, it is evident that 1-methyl-2-carbethoxy-3-phenyl-1-thia-4-azanaphthalene is an alias for a molecule more properly represented by a name emphasizing its zwitterionic character.

Reaction between 2,2'-Dithiodianiline and Activated Alkynes. Synthesis of 4H-1,4-Benzothiazines

Liso, Gaetano,Trapani, Giuseppe,Reho, Antonia,Latrofa, Andrea,Loiodice, Fulvio

, p. 567 - 572 (2007/10/02)

By the title reaction acetylenic esters (2a-c), ketones (2d-g), and the nitrile (2h) gave in all cases the corresponding 4H-1,4-benzothiazines (3) together with other products whose nature depends on the alkyne used.Thus benzothiazoline and/or benzothiazole, benzothiazepine, and vinylsulphides were obtained in the representative cases (2c, f, h) studied in detail.Some of these latter compounds have been independently synthesised by reaction of 2-aminobenzenethiol with corresponding alkyne (2).In particular conditions by the reactions between 2,2'-dithiodianiline (1) and alkynes (2f, d) we isolated bisenamine compounds (19) and (20) respectively and their intermediacy in formation of the corresponding benzothiazines (3f) and (3d) was achieved.The mechanisms of the observed reactions are also suggested.

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