5511-18-2 Usage
Description
1-Adamantanecarboxamide is a white solid with unique chemical properties that make it suitable for various applications, particularly in the field of virology and pharmaceuticals.
Uses
Used in Virology:
1-Adamantanecarboxamide is used as an antiviral agent for the reproduction of Sindbis virus strains that are sensitive and resistant to its effects. This application is significant in understanding the behavior of these virus strains and potentially developing targeted treatments.
Used in Pharmaceutical Industry:
1-Adamantanecarboxamide is used as a key component in the development of drugs targeting specific virus strains. Its antiviral properties make it a valuable asset in the creation of medications aimed at combating viral infections, particularly those resistant to conventional treatments.
Used in Chemical Research:
As a white solid with distinct chemical properties, 1-Adamantanecarboxamide is also used in chemical research to study its interactions with other compounds and to explore its potential applications in various chemical processes and reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 5511-18-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,1 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5511-18:
(6*5)+(5*5)+(4*1)+(3*1)+(2*1)+(1*8)=72
72 % 10 = 2
So 5511-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO/c12-10(13)11-4-7-1-8(5-11)3-9(2-7)6-11/h7-9H,1-6H2,(H2,12,13)
5511-18-2Relevant articles and documents
Metal-free one-pot oxidative conversion of benzylic alcohols and benzylic halides into aromatic amides with molecular iodine in aq ammonia, and hydrogen peroxide
Ohmura, Ryosuke,Takahata, Misato,Togo, Hideo
experimental part, p. 4378 - 4381 (2010/09/12)
Various primary alcohols, particularly benzylic alcohols, could be converted into the corresponding aromatic amides in good yields in a one-pot manner by treatment with molecular iodine in aq. NH3, followed by reaction with ～30% aq H2O2. Similarly, various benzylic halides could be also converted into the corresponding aromatic amides in good yields in a one-pot manner by treatment with molecular iodine in aq NH3, followed by reaction with ～30% aq H2O 2. The present reactions involve the metal-free one-pot oxidative conversion of benzylic alcohols and benzylic halides into the corresponding aromatic amides, respectively.
