79607-21-9 Usage
Chemical class
Pyrrolidine-2,5-dione derivative
Pharmacological effects
Non-narcotic analgesic and non-steroidal anti-inflammatory drug
Uses
Treating mild to moderate pain and inflammation, such as headache, dental pain, and musculoskeletal pain
Mechanism of action
Inhibits the synthesis of prostaglandins, which are involved in the transmission of pain and inflammation signals
Limitations
Potential for severe adverse effects, including gastrointestinal bleeding, hepatotoxicity, and renal failure
Clinical use
Not commonly used due to its side effects
Structure
Contains a pyrrolidine-2,5-dione core with a 2-oxo-1,2-diphenylethyl group attached to the nitrogen atom
Appearance
Likely a solid, as most organic compounds with similar structures are solids at room temperature
Check Digit Verification of cas no
The CAS Registry Mumber 79607-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,0 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79607-21:
(7*7)+(6*9)+(5*6)+(4*0)+(3*7)+(2*2)+(1*1)=159
159 % 10 = 9
So 79607-21-9 is a valid CAS Registry Number.
79607-21-9Relevant academic research and scientific papers
Wei, Ting,Zeng, Yongming,He, Wei,Geng, Lili,Hong, Liang
, p. 383 - 385 (2019)
A facile transformation of alkynes into α-amino ketones by an N-bromosuccinimide-mediated one-pot cascade strategy is described. A variety of α-amino ketones are obtained in moderate to good yields under mild conditions. To overcome the multi-step synthesis, N-bromosuccinimide is involved in multiple tasks, playing a key role in the reaction course.
One-pot cascade leading to direct α-imidation of ketones by a combination of N-bromosuccinimide and 1,8-diazabicyclo[5.4.1]undec-7-ene
Wei, Ying,Lin, Shaoxia,Liang, Fushun
experimental part, p. 4202 - 4205 (2012/10/08)
A one-pot cascade transformation of ketones into α-imidoketones has been developed, in which N-bromosuccinimide (NBS) provides both electrophilic bromine and nucleophilic nitrogen sources, and diazabicyclo[5.4.1]undec-7-ene (DBU) functions as a base and a
