179894-05-4 Usage
Structure
Cyclic β-lactam derivative with a four-membered ring
Usage
Building block in organic synthesis and pharmaceutical research
Applications
Development of new pharmaceutical drugs
Reactivity
Unique structure and reactivity for preparation of functionalized molecules
Biological activities
Potential antimicrobial, antifungal, and antiviral properties
Derivatives
Studied for their various biological properties
Versatility
Promising applications in medicinal and synthetic chemistry
Check Digit Verification of cas no
The CAS Registry Mumber 179894-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,8,9 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 179894-05:
(8*1)+(7*7)+(6*9)+(5*8)+(4*9)+(3*4)+(2*0)+(1*5)=204
204 % 10 = 4
So 179894-05-4 is a valid CAS Registry Number.
179894-05-4Relevant academic research and scientific papers
Synthesis of N-substituted azetidin-3-ones
Marchand, Alan P.,Devasagayaraj, Arokiasamy
, p. 885 - 890 (2007/10/03)
Addition of RC(O)Cl (R = OEt, Me, or Ph) across the highly strained N- C(3) σ-bond in 3-bromomethyl-1-azabicyclo[1.1.0]butane (1) afforded the corresponding N-acyl-3-bromomethyl-3-chloroazetidines (2a-2c, respectively). Subsequent zinc promoted eliminativ
Acylative dealkylation of N-tert-butyl-3-substituted azetidines: Facile access to [1.1.0]azabicyclobutane, 3-hydroxyazetidinium hydrochloride, and 3-azetidinones
Dave, Paritosh R.
, p. 5453 - 5455 (2007/10/03)
A novel acylative dealkylation of N-tert-butylazetidines and its application to the facile high-yield syntheses of [1.1.0]azabicyclobutane, 3-hydroxyazetidinium hydrochloride, and 3-azetidinones is described.
