132813-86-6 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 17 carbon (C) atoms, 14 hydrogen (H) atoms, and 5 oxygen (O) atoms.
Explanation
1,3-Benzodioxole-5-acetic acid, 6-benzoyl- is a derivative of benzodioxole and acetic acid, with a benzoyl group attached to the 6th position of the benzodioxole ring.
Explanation
The compound contains three main functional groups benzodioxole, which is a fused ring system consisting of a benzene ring and an oxygen-containing heterocycle; acetic acid, which is a carboxylic acid; and benzoyl, which is an aromatic ketone.
Explanation
1,3-Benzodioxole-5-acetic acid, 6-benzoylis commonly used as a precursor in the synthesis of various pharmaceuticals and organic compounds due to its unique chemical structure and reactivity.
Explanation
Studies have shown that 1,3-Benzodioxole-5-acetic acid, 6-benzoyl- has potential pharmacological properties, including the ability to reduce inflammation and inhibit tumor growth.
Explanation
Due to its unique structure and properties, 1,3-Benzodioxole-5-acetic acid, 6-benzoylhas been investigated for its potential use as a building block in the development of new drugs and agrochemicals, which could have various applications in medicine and agriculture.
Chemical structure
1,3-Benzodioxole-5-acetic acid, 6-benzoyl-
Functional groups
Benzodioxole, acetic acid, and benzoyl
Application
Pharmaceutical and organic compound synthesis
Pharmacological properties
Anti-inflammatory and anti-tumor activities
Potential use
Building block for new drugs and agrochemicals
Check Digit Verification of cas no
The CAS Registry Mumber 132813-86-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,1 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132813-86:
(8*1)+(7*3)+(6*2)+(5*8)+(4*1)+(3*3)+(2*8)+(1*6)=116
116 % 10 = 6
So 132813-86-6 is a valid CAS Registry Number.
132813-86-6Relevant academic research and scientific papers
Novel α-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) receptor antagonists of 2,3-benzodiazepine type: Chemical synthesis, in vitro characterization, and in vivo prevention of acute neurodegeneration
Elger, Bernd,Huth, Andreas,Neuhaus, Roland,Ottow, Eckard,Schneider, Herbert,Seilheimer, Bernd,Turski, Lechoslaw
, p. 4618 - 4627 (2007/10/03)
Under pathophysiological conditions, α-amino-3-hydroxy-5-methyl-4- isoxazole propionate (AMPA) receptor activation is considered to play a key role in several disorders of the central nervous system. In the search for AMPA receptor antagonists, the synthe
Method for the production of imidazo-(1,2-C)(2,3)-benzodiazepines and intermediates in the production thereof
-
Page 3; 5, (2008/06/13)
The invention relates to a method for the preparation of compound of formula (1). The invention further relates to the previously unknown compounds of formulas (5 and 6) as intermediates in the production of benzodiazepines of formula (1).
Diphenylimidazo [1, 2-c] [2, 3] Benzodiazepin and their production method for production of the intermediate product
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Page/Page column 14-15, (2008/06/13)
The invention relates to a method for the preparation of compound of formula (1). The invention further relates to the previously unknown compounds of formulas (5 and 6) as intermediates in the production of benzodiazepines of formula (1).
2-Benzopyran-3-ones Stabilised by Alkoxy Substituents
Bradshaw, David P.,Jones, David W.,Tideswell, John
, p. 169 - 173 (2007/10/02)
In contrast to the corresponding compounds lacking alkoxy substituents, the 2-benzopyran-3-ones 5, 6, 7 and 9 are stable and easily isolated.In contrast to the 6-methoxy derivative 7, the 7-methoxy isomer 8 cannot be isolated; the stabilising effect of th
