119326-94-2 Usage
General Description
1-(N,N-dibenzylamino)cyclopropanol is a chemical compound that consists of a cyclopropane ring with a hydroxy group and a dibenzylamino group attached to it. It is a tertiary amine derivative and is commonly used as a building block in organic synthesis. 1-(N,N-dibenzylaMino)cyclopropanol has been studied for its potential pharmaceutical applications due to its unique structural properties. The dibenzylamino group provides steric hindrance and electron density, which can influence the reactivity and selectivity of chemical reactions involving this compound. Additionally, the cyclopropane ring is known for its high strain energy, and its presence in this molecule may contribute to its biological activity. Overall, 1-(N,N-dibenzylamino)cyclopropanol is a versatile chemical that has potential applications in drug discovery and organic synthesis.
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.
