119326-94-2 Usage
Uses
Used in Organic Synthesis:
1-(N,N-dibenzylamino)cyclopropanol is used as a building block for the synthesis of various organic compounds due to its unique structural properties, including the steric hindrance and electron density provided by the dibenzylamino group, which can affect the reactivity and selectivity of reactions.
Used in Pharmaceutical Applications:
1-(N,N-dibenzylamino)cyclopropanol is used as a potential candidate in drug discovery for its unique structural properties and biological activity. 1-(N,N-dibenzylaMino)cyclopropanol's cyclopropane ring, with its high strain energy, may contribute to its potential therapeutic effects, making it a subject of interest for further research and development in the pharmaceutical industry.
Used in Drug Discovery:
1-(N,N-dibenzylamino)cyclopropanol is utilized in drug discovery processes to explore its potential as a precursor or intermediate in the development of new pharmaceuticals. Its unique structural features and reactivity make it a promising candidate for creating novel drug molecules with specific therapeutic targets.
Check Digit Verification of cas no
The CAS Registry Mumber 119326-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,3,2 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 119326-94:
(8*1)+(7*1)+(6*9)+(5*3)+(4*2)+(3*6)+(2*9)+(1*4)=132
132 % 10 = 2
So 119326-94-2 is a valid CAS Registry Number.
119326-94-2Relevant articles and documents
Decarboxylation of 1-Aminocyclopropanecarboxylic Acid and Its Derivatives
Vaidyanathan, Ganesan,Wilson, Joseph W.
, p. 1810 - 1815 (2007/10/02)
The question of whether the title compounds could be decarboxylated to cyclopropanone derivatives was answered in the affirmative by the following observations. (1) Compound 11a was decarboxylated by 1,2,3-indantrione in acetonitrile, benzene, or methanol.The initially formed intermediate could be trapped by N-phenylmaleimide (to form 3), by diethyl azodicarboxylate (to form an unstable adduct), by ninhydrin itself (to form 5) or by a proton (in methanol, to form 8). (2) Compound 11d was decarboxylated by phenylbis(trifluoroacetato-O)iodine to yield carbinolamine 12d.cis-2,3-Dideuterio-11d yielded cis-2,3-dideuterio-12d under the same conditions. (3) ACC was decarboxylated by phenanthroquinone to yield oxazole 9, probably by way of oxazoline 10.
