39096-80-5 Usage
Uses
Used in Pharmaceutical Industry:
2,2-Dichloro-N-(1-phenylethyl)acetamide is used as a topical antifungal and antibacterial agent for the treatment of various skin infections. It is particularly effective against athlete's foot and ringworm, which are common fungal infections affecting the skin.
As a Topical Antifungal Agent:
2,2-Dichloro-N-(1-phenylethyl)acetamide is used as a topical antifungal agent to inhibit the growth of fungi on the skin. It is commonly formulated into creams or ointments, which are applied directly to the affected area to treat fungal infections.
As a Topical Antibacterial Agent:
2,2-Dichloro-N-(1-phenylethyl)acetamide also serves as a topical antibacterial agent, helping to combat bacterial infections on the skin. Its ability to inhibit bacterial growth makes it a useful component in formulations designed to treat skin infections caused by bacteria.
For Skin Infection Treatment:
2,2-Dichloro-N-(1-phenylethyl)acetamide is used for the treatment of various skin infections, including fungal and bacterial infections. Its effectiveness in reducing and eliminating infections makes it a safe and reliable option when used as directed.
Check Digit Verification of cas no
The CAS Registry Mumber 39096-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,9 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39096-80:
(7*3)+(6*9)+(5*0)+(4*9)+(3*6)+(2*8)+(1*0)=145
145 % 10 = 5
So 39096-80-5 is a valid CAS Registry Number.
39096-80-5Relevant academic research and scientific papers
Stereoselective synthesis of racemic α-amino-acid derivatives with a β-lactam skeleton: Application of the Staudinger reaction to chiral imines of methyl glyoxylate
Barreau, Michel,Commercon, Alain,Mignani, Serge,Mouysset, Dominique,Perfetti, Patricia,Stella, Lucien
, p. 11501 - 11516 (2007/10/03)
Selected imines of methyl glyoxylate act as good partners in the Staudinger cycloaddition reaction with a series of substituted ketenes. The cis stereoselectivity is almost complete with electron-donor substituted ketenes, but the asymmetric induction is low when imines derived from chiral l-aryl-ethylamines are used.
