501939-11-3 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 8 carbon (C) atoms, 11 hydrogen (H) atoms, 1 nitrogen (N) atom, and 1 oxygen (O) atom.
Explanation
This is the systematic name of the compound, which provides information about its structure and stereochemistry.
Explanation
The compound is derived from a hexahydroindolizine, which is a bicyclic structure containing a nitrogen atom.
Explanation
The compound has been studied for its potential pharmacological properties, which include acting as an antioxidant and possibly being useful in the treatment of neurodegenerative diseases.
Explanation
Due to its unique structure and properties, the compound may have potential applications in the fields of organic synthesis and medicinal chemistry.
Explanation
More research is required to fully understand the properties and potential applications of this compound, as its current knowledge is limited.
Structure
Hexahydroindolizine derivative
Stereochemistry
(1S,2S,8aR)
Pharmacological Properties
Potential antioxidant and therapeutic applications in neurodegenerative diseases
Applications
Organic synthesis and medicinal chemistry
Research Status
Further research needed
Check Digit Verification of cas no
The CAS Registry Mumber 501939-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,9,3 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 501939-11:
(8*5)+(7*0)+(6*1)+(5*9)+(4*3)+(3*9)+(2*1)+(1*1)=133
133 % 10 = 3
So 501939-11-3 is a valid CAS Registry Number.
501939-11-3Relevant articles and documents
O-(2-oxopyrrolidin-5-yl)trichloroacetimidates as amidoalkylating agents - Synthesis of (+)-lentiginosine
El-Nezhawy, Ahmed O. H.,El-Diwani, Hoda I.,Schmidt, Richard R.
, p. 4137 - 4142 (2002)
N-α-Hydroxyalkylamides 6a,b, readily available from L-tartrate, with trichloroacetonitrile furnish O-(2-oxopyrrolidin-5-yl)trichloroacetimidates 3a,b. α-Amido-alkylation studies of 3a,b with allyl-trimethylsilane and electron-rich benzene derivatives as C-nucleophiles afforded 5-allyl- and 5-aryl-2-pyrrolidinones 2a,b, 7a,b, and 8-10. The target compound (+)-1 and its epimer 15 were readily obtained from 1,5-diallyl-2-pyrrolidinones 2b and 7b, respectively, via ring-closing metathesis, amide group reduction, and CC-double bond hydrogenation. Wiley-VCH Verlag GmbH & Co KGaA, 69451 Weinheim, Germany, 2002.
