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The chemical compound "C15H13BrN2O3" is a brominated organic molecule with a molecular formula indicating the presence of 15 carbon atoms, 13 hydrogen atoms, 1 bromine atom, 2 nitrogen atoms, and 3 oxygen atoms. C15H13BrN2O3 likely belongs to a class of organic compounds known as brominated nitro derivatives, which are characterized by the presence of a bromine atom and nitro groups (NO2). The structure of C15H13BrN2O3 would feature a complex arrangement of these atoms, potentially with a benzene ring or other aromatic systems, given the number of carbon and hydrogen atoms. The bromine atom could be attached to a carbon in the aromatic system, and the nitro groups could be substituents on the ring or attached to other parts of the molecule. The presence of nitrogen atoms suggests that the compound may have amide or amine functional groups, which could contribute to its reactivity and properties. Overall, C15H13BrN2O3 represents a complex organic molecule with potential applications in various fields, such as pharmaceuticals or chemical research, depending on its specific structure and properties.

1567-02-8

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1567-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1567-02-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1567-02:
(6*1)+(5*5)+(4*6)+(3*7)+(2*0)+(1*2)=78
78 % 10 = 8
So 1567-02-8 is a valid CAS Registry Number.

1567-02-8Relevant academic research and scientific papers

Specific inhibitors of puromycin-sensitive aminopeptidase with a 3-(halogenated phenyl)-2,4(1H,3H)-quinazolinedione skeleton

Matsumoto, Yotaro,Noguchi-Yachide, Tomomi,Nakamura, Masaharu,Mita, Yusuke,Numadate, Akiyoshi,Hashimoto, Yuichi

, p. 1449 - 1463 (2013/08/23)

Specific puromycin-sensitive aminopeptidase (PSA) inhibitors with a 3-(halogenated phenyl)-2,4(1H,3H)-quinazolinedione skeleton were prepared and their structure-activity relationships were investigated. The nature (F, Cl or Br), number and position(s) of the halogen atom(s) introduced into the 3-phenyl group were concluded to be critical determinants of the inhibitory activity.

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