59507-55-0 Usage
General Description
3-Bromo-N-cyclohexylbenzamide is an organic compound that consists of a benzene ring attached to a cyclohexyl group and a bromine atom, as well as an amide function. It is a white to off-white crystalline solid that is sparingly soluble in water but soluble in many organic solvents. 3-Bromo-N-cyclohexylbenzamide is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also known to possess anti-inflammatory and analgesic properties, making it a potential candidate for drug development. Additionally, 3-Bromo-N-cyclohexylbenzamide has been studied for its potential antibacterial and antifungal activities, and it may also have applications in the field of material science and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 59507-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,0 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59507-55:
(7*5)+(6*9)+(5*5)+(4*0)+(3*7)+(2*5)+(1*5)=150
150 % 10 = 0
So 59507-55-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H16BrNO/c14-11-6-4-5-10(9-11)13(16)15-12-7-2-1-3-8-12/h4-6,9,12H,1-3,7-8H2,(H,15,16)
59507-55-0Relevant articles and documents
AMINE DERIVATIVE COMPOUNDS FOR TREATING OPHTHALMIC DISEASES AND DISORDERS
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Paragraph 2079, (2016/08/07)
Provided are amine derivative compounds, pharmaceutical compositions thereof, and methods of treating ophthalmic diseases and disorders, such as age-related macular degeneration and Stargardt's Disease, using said compounds and compositions.
Radical mediated-direct conversion of aldehydes into acid bromides
Kang, Dong Ho,Joo, Tae Young,Chavasiri, Warinthorn,Jang, Doo Ok
, p. 285 - 287 (2007/10/03)
A method of preparing acid bromides directly from aldehydes with Br3CCO2Et under radical conditions was developed. Aromatic aldehydes with electron-donating group were found to be more reactive than aromatic aldehydes with electron-w
