3405-48-9 Usage
Uses
Used in Organic Synthesis:
N-(1-Adamantyl)formamide is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the development of new compounds and materials.
Used in Pharmaceutical Production:
As an intermediate, N-(1-Adamantyl)formamide plays a crucial role in the production of pharmaceuticals, aiding in the synthesis of drug molecules that can address a range of health conditions.
Used in Agrochemical Production:
N-(1-Adamantyl)formamide is also utilized as an intermediate in the creation of agrochemicals, which are essential for enhancing crop protection and yield.
Used in Anti-inflammatory Applications:
Due to its anti-inflammatory properties, N-(1-Adamantyl)formamide is being explored for its potential use in treating conditions characterized by inflammation, offering a new avenue for therapeutic intervention.
Used in Anti-cancer Applications:
N-(1-Adamantyl)formamide's anti-cancer properties are under investigation for its potential to be developed into a treatment for various types of cancer, providing a novel approach to cancer therapy.
Used in Disease Treatment Research:
Ongoing research is being conducted to understand the full potential benefits and risks of N-(1-Adamantyl)formamide in treating a variety of diseases, with the aim of expanding its applications in the medical field.
Check Digit Verification of cas no
The CAS Registry Mumber 3405-48-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3405-48:
(6*3)+(5*4)+(4*0)+(3*5)+(2*4)+(1*8)=69
69 % 10 = 9
So 3405-48-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO/c13-7-12-11-4-8-1-9(5-11)3-10(2-8)6-11/h7-10H,1-6H2,(H,12,13)
3405-48-9Relevant academic research and scientific papers
The Invention of Radical Reactions. 32. Radical Deoxygenations, Dehalogenations, and Deaminations with Dialkyl Phosphites and Hypophosphorous Acid as Hydrogen Sources
Barton, Derek H. R.,Jang, Doo Ok,Jaszberenyi, Joseph Cs.
, p. 6838 - 6842 (2007/10/02)
Reagents, containing a P-H bond, such as dimethyl phosphite, diethyl phosphite, hypophosphorous acid and various salts of hypophosphorous acid are effective radical reducing agents for organic halides, thionoesters, and isocyanides affording high yields of the corresponding hydrocarbons.Reduction of tertiary phenyl selenides and tertiary nitro compounds are not efficient under these conditions.Olefination of 1,2-diols is also accomplished via the corresponding thiocarbonyl derivatives using hypophosphorous acid and triethylamine in the presence of a suitable "sacrifical olefin" im moderate to good yields.
Hypophosphorous acid and its salts: New reagents for radical chain deoxygenation, dehalogenation and deamination
Barton,Jang,Jaszberenyi
, p. 5709 - 5712 (2007/10/02)
Thionocarbonates and xanthates of alcohols, bromides, iodides and isonitriles can be transformed to the corresponding hydrocarbons with hypophosphorous acid or its salts in radical chain reactions.
