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N-(4,5-dihydronaphtho[1,2-d][1,3]thiazol-2-yl)acetamide is a complex organic compound with the molecular formula C12H10N2OS. It is characterized by a dihydronaphtho[1,2-d][1,3]thiazol-2-yl group attached to an acetamide moiety. N-(4,5-dihydronaphtho[1,2-d][1,3]thiazol-2-yl)acetamide is known for its potential applications in pharmaceutical research, particularly as a building block for the synthesis of various bioactive molecules. Its structure features a fused ring system with a thiazole ring and a dihydronaphtho core, which contributes to its unique chemical properties. The compound's specific role in drug development or other applications is not detailed here, but its structure suggests it may be involved in the creation of compounds with specific biological activities.

7496-70-0

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7496-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7496-70-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7496-70:
(6*7)+(5*4)+(4*9)+(3*6)+(2*7)+(1*0)=130
130 % 10 = 0
So 7496-70-0 is a valid CAS Registry Number.

7496-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4,5-dihydrobenzo[e][1,3]benzothiazol-2-yl)acetamide

1.2 Other means of identification

Product number -
Other names HMS1414G09

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:7496-70-0 SDS

7496-70-0Downstream Products

7496-70-0Relevant academic research and scientific papers

Synthesis and biological evaluation of 2-aminothiazoles and their amide derivatives on human adenosine receptors. Lack of effect of 2-aminothiazoles as allosteric enhancers

Goeblyoes, Aniko,Santiago, Sabrina Neves,Pietra, Daniele,Mulder-Krieger, Thea,Kuenzel, Jacobien Von Frijtag Drabbe,Brussee, Johannes,Ijzerman, Adriaan P.

, p. 2079 - 2087 (2005)

A number of 2-aminothiazoles (2a-e) and their amide derivatives (4-10) were prepared. The 2-aminothiazoles themselves were tested as allosteric enhancers of agonist binding to human adenosine A1 receptors. In a variety of experimental set-ups the compounds did not show any such effect, in contrast to earlier findings by another research group. Subsequently the 2-aminothiazoles were used as intermediates in the synthesis of a number of amide derivatives of either aromatic (4-6) or aliphatic nature (7-10). Some of the compounds emerged as moderately active antagonists on human adenosine A1 and/or A 2A receptors with lower or negligible potency at adenosine A 3 receptors.

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