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

90252-70-3

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90252-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90252-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,5 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90252-70:
(7*9)+(6*0)+(5*2)+(4*5)+(3*2)+(2*7)+(1*0)=113
113 % 10 = 3
So 90252-70-3 is a valid CAS Registry Number.

90252-70-3SDS

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 benzyl 3-methyl-4H-1,4-benzothiazine-2-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:90252-70-3 SDS

90252-70-3Downstream Products

90252-70-3Relevant academic research and scientific papers

One-pot multi-component approach to the synthesis of 1,4-benzothiazines in aqueous media

Sheibani, Hassan,Islami, Mohammad Reza,Hassanpour, Avid,Saidi, Kazem

, p. 13 - 20 (2008/12/21)

A new and rapid synthetic strategy for the oxidative cyclocondensation of 2-aminobenzenethiol and 1,3-dicarbonyls has been developed in order to obtain 2,3-disubstituted 1,4-benzothiazines at ambient temperature and in aqueous media. A mechanism is presen

Reactions of 1,2-diaza-1,3-dienes with thiol derivatives: a versatile construction of nitrogen/sulfur containing heterocycles

Attanasi, Orazio A.,Filippone, Paolino,Lillini, Samuele,Mantellini, Fabio,Nicolini, Simona,de los Santos, Jesús M.,Ignacio, Roberto,Aparicio, Domitila,Palacios, Francisco

, p. 9264 - 9274 (2008/12/21)

The synthesis of substituted 2,3-dihydro-1,4-thiazines, fused cycloalkyl-1,4-thiazines, 1,4-benzothiazines and fused cycloalkyl-1,4-benzothiazines by 1,4-addition of 1,2-aminothiols to 1,2-diaza-1,3-dienes bearing carboxylate, carboxamide, or phosphorylated groups and subsequent internal heterocyclization is described. The reaction of carboxylated 1,2-diaza-1,3-butadienes with 2-(butylamino)ethanethiol affords 1,4-thiazinan-3-ones. The solid-phase reaction of polymer-bound 1,2-diaza-1,3-butadienes with 1,2-aminothiols produces 2,3-dihydro-1,4-thiazines and 1,4-benzothiazines.

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