116071-95-5 Usage
Molecular weight
326.26 g/mol the mass of one mole of the compound.
Hexahydro derivative
The compound has six hydrogen atoms added to the pyrrolizine core, making it a hexahydro derivative.
Ethyl ester
The compound contains an ethyl group (C2H5) attached to the carboxylic acid functional group (-COOH).
Phenylseleno group
The presence of a phenyl group (C6H5) bonded to a selenium atom (Se) in the compound.
Pyrrolizine core
The compound has a five-membered nitrogen-containing ring structure.
Use in organic synthesis
The compound is commonly used as a building block in organic synthesis for creating diverse chemical structures.
Pharmaceutical intermediate
The compound serves as an intermediate in the synthesis of pharmaceuticals.
Potential bioactive properties
Due to its unique structure, the compound may have potential bioactive properties.
Caution with handling
The compound contains a selenium moiety, which may have potential safety and environmental concerns. It should be handled with care and its safety and environmental impact should be assessed.
Check Digit Verification of cas no
The CAS Registry Mumber 116071-95-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,7 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116071-95:
(8*1)+(7*1)+(6*6)+(5*0)+(4*7)+(3*1)+(2*9)+(1*5)=105
105 % 10 = 5
So 116071-95-5 is a valid CAS Registry Number.
116071-95-5Relevant academic research and scientific papers
A Novel Synthesis of Pyrrolizidine Alkaloids by Means of an Intramolecular Carbenoid Displacement (ICD) Reaction
Kametani, Tetsuji,Yukawa, Hirotaka,Honda, Toshio
, p. 833 - 838 (2007/10/02)
The pyrrolizidine alkaloids, (+/-)-trachelanthamidine, (+/-)-isoretronecanol, and (+/-)-supinidine were synthesized by using an intramolecular carbenoid displacement (ICD) reaction of the diazo-sulphide or the diazo-selenide derivatives as a key step.
