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N-(4-methoxyphenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine is an organic compound with a unique chemical structure that features a thiazin ring fused with a dihydro ring and a 4-methoxyphenyl group. N-(4-methoxyphenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine is known for its potential applications in the synthesis of various heterocycles, particularly benzimidazole-fused ones, due to its reactive functional groups and structural characteristics.

61452-16-2

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61452-16-2 Usage

Uses

Used in Pharmaceutical Industry:
N-(4-methoxyphenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine is used as a synthetic intermediate for the preparation of benzimidazole-fused heterocycles, which are important in the development of new pharmaceutical compounds. These heterocycles have been found to possess a range of biological activities, including anti-cancer, anti-inflammatory, and anti-microbial properties, making them valuable for the creation of novel therapeutic agents.
Used in Chemical Research:
In the field of chemical research, N-(4-methoxyphenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine serves as a versatile building block for the synthesis of complex organic molecules. Its unique structure allows for further functionalization and modification, enabling the development of new compounds with potential applications in various industries, such as materials science, agrochemistry, and environmental science.
Used in Material Science:
N-(4-methoxyphenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine can be utilized as a component in the development of advanced materials, such as organic electronics, sensors, and optoelectronic devices. N-(4-methoxyphenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine's electronic properties and structural flexibility make it a promising candidate for the design of novel materials with improved performance and functionality.

Check Digit Verification of cas no

The CAS Registry Mumber 61452-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,5 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61452-16:
(7*6)+(6*1)+(5*4)+(4*5)+(3*2)+(2*1)+(1*6)=102
102 % 10 = 2
So 61452-16-2 is a valid CAS Registry Number.

61452-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-methoxyphenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine

1.2 Other means of identification

Product number -
Other names p-anisidino-2 4H dihydro-5,6 thiazine-1,3

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:61452-16-2 SDS

61452-16-2Downstream Products

61452-16-2Relevant academic research and scientific papers

Aminothiazines et aminothiazoles analogues ouverts du levamisole: synthese et approche du mode d'action nematicide

Caujolle, Raymond,Amarouch, Hamid,Payard, Marc,Loiseau, Philippe R.,Bories, Christian,et al.

, p. 287 - 292 (2007/10/02)

New compounds with thiazoline or dihydrothiazine rings substituted by alkylamino or arylamino groups were synthesized and screened in vitro against three Nematodes.Inhibition of fumarate-reductase activity was also evaluated.For all in vitro anti-parasitic tests, dihydrothiazines were more potent than corresponding thiazolines derivatives, however, thiazolines showed a greater inhibition of fumarate-reductase.

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