5111-73-9 Usage
Appearance
White to off-white solid
Solubility
Sparingly soluble in water
Uses
a. Intermediate in the synthesis of pharmaceuticals and agrochemicals
b. Potential use in the production of dyes and pigments
Biological activities
a. Anti-inflammatory properties
b. Antifungal properties
Potential applications
Drug development and medicinal applications
Check Digit Verification of cas no
The CAS Registry Mumber 5111-73-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,1 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5111-73:
(6*5)+(5*1)+(4*1)+(3*1)+(2*7)+(1*3)=59
59 % 10 = 9
So 5111-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-4,6-7,10H,5H2,(H,12,13)
5111-73-9Relevant academic research and scientific papers
Hydroxide ion as electron source for photochemical Birch-type reduction and photodehalogenation
Yoshimi, Yasuharu,Ishise, Akihiro,Oda, Hiromu,Moriguchi, Yousuke,Kanezaki, Hiroki,Nakaya, Yukari,Katsuno, Kayoko,Itou, Tatsuya,Inagaki, Sho,Morita, Toshio,Hatanaka, Minoru
, p. 3400 - 3404 (2008/09/21)
The photochemical Birch-type reduction of arenes and the photodehalogenation of haloarenes by a hydroxide ion that acted as an electron source occurred in 2-PrOH. The efficiency of these photoreactions was dependent on the nature of the substrate, the concentration of NaOH, and the solvent used. These photoreactions provide an environmentally friendly method for the reduction of aromatic rings and dehalogenation.
