501939-10-2 Usage
Hexahydroindolizine derivative
A type of chemical compound derived from indolizine
This indicates that the compound is a modified version of the indolizine structure, with six hydrogen atoms added to the molecule.
Stereochemistry
(1S,2S,8aS)
This refers to the specific arrangement of atoms in the molecule, which can influence its properties and potential applications.
Biological activity
Likely exhibits biological activity
As a derivative of indolizine, this compound may have potential biological effects, although further research is needed to confirm this.
Potential applications
Pharmaceutical or organic synthesis
Due to its unique structure and potential biological activity, this compound may have uses in the development of pharmaceuticals or as an intermediate in organic synthesis.
Research and study
Not widely studied or commercially available
This compound is not well documented in the literature, and further research is needed to fully understand its role and potential in the field of chemistry and medicine.
CAS Registry Number
9CI
This is a unique identifier assigned to the compound by the Chemical Abstracts Service, which can be used to search for information about the compound in scientific databases.
Check Digit Verification of cas no
The CAS Registry Mumber 501939-10-2 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 501939-10:
(8*5)+(7*0)+(6*1)+(5*9)+(4*3)+(3*9)+(2*1)+(1*0)=132
132 % 10 = 2
So 501939-10-2 is a valid CAS Registry Number.
501939-10-2Relevant 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 (2007/10/03)
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.
