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AKOS B018378, also known as 5-Azido-2,4-dinitro-benzoic acid, is a potent explosive chemical compound with potential applications in military and industrial settings. It is highly reactive and can be triggered by heat, shock, or friction. Due to its explosive properties, AKOS B018378 must be handled with extreme care and is subject to stringent regulations and controls to prevent misuse and accidental harm. It is a dangerous and potentially lethal substance that demands cautious handling and storage.

56661-83-7

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56661-83-7 Usage

Uses

Used in Military Applications:
AKOS B018378 is used as an explosive compound for its high reactivity and ability to be detonated by heat, shock, or friction. It is employed in military applications for its powerful explosive capabilities, providing a significant advantage in various military operations.
Used in Industrial Applications:
In the industrial sector, AKOS B018378 is used as a component in the manufacturing of explosives and pyrotechnic devices. Its high reactivity and explosive properties make it suitable for various industrial applications, such as demolition, mining, and construction.

Check Digit Verification of cas no

The CAS Registry Mumber 56661-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,6 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56661-83:
(7*5)+(6*6)+(5*6)+(4*6)+(3*1)+(2*8)+(1*3)=147
147 % 10 = 7
So 56661-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H7NO3S2/c13-9-8(17-11(16)12-9)5-6-3-1-2-4-7(6)10(14)15/h1-5H,(H,14,15)(H,12,13,16)

56661-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(E)-(2-Mercapto-4-oxo-1,3-thiazol-5(4H)-ylidene)methyl]benzoic acid

1.2 Other means of identification

Product number -
Other names 2-(4-oxo-2-thioxo-thiazolidin-5-ylidenemethyl)-benzoic acid

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:56661-83-7 SDS

56661-83-7Relevant academic research and scientific papers

Isothiocoumarin-3-carboxylic acid derivatives: Synthesis, anticancer and antitrypanosomal activity evaluation

Kaminskyy, Danylo,Kryshchyshyn, Anna,Nektegayev, Ihor,Vasylenko, Olexandr,Grellier, Philippe,Lesyk, Roman

, p. 57 - 66 (2014/03/21)

A series of new isothiocoumarin-3-carboxylic acids derivatives had been obtained based on the 5-arylidenerhodanines hydrolysis. Anticancer activity screening allowed identification of 7,8-dimethoxy-1-oxo-1H-isothiochromene-3- carboxylic acid (4-phenylthia

The synthesis and SAR of rhodanines as novel class C β-lactamase inhibitors

Grant, Eugene B.,Guiadeen, Deodialsingh,Baum, Ellen Z.,Foleno, Barbara D.,Jin, Haiyong,Montenegro, Deborah A.,Nelson, Erin A.,Bush, Karen,Hlasta, Dennis J.

, p. 2179 - 2182 (2007/10/03)

β-Lactam antibiotics such as the cephalosporins and penicillins have diminished clinical effectiveness due to the hydrolytic activity of diverse β-lactamases, especially those in molecular classes A and C. A structure-activity relationship (SAR) study of

1-Oxo-1H-2-benzothiopyran-3-carboxylic acid derivatives

-

, (2008/06/13)

The method comprises administering to an animal a novel pharmaceutical composition containing a substituted-1-oxo-1H-2-benzothiopyran-3-carboxylic acid to inhibit antigen-antibody reaction in said animal. Representative of the compounds that can be used i

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