216392-65-3 Usage
Description
1H-Pyrrolizine-7a(5H)-carboxylic acid, tetrahydro-3-oxo-, phenylmethyl ester is a chemical compound with the molecular formula C16H15NO3. It is a phenylmethyl ester of pyrrolizine-carboxylic acid, often utilized as a building block in the synthesis of pharmaceuticals and other organic compounds.
Uses
Used in Pharmaceutical Industry:
1H-Pyrrolizine-7a(5H)-carboxylic acid, tetrahydro-3-oxo-, phenylmethyl ester is used as a building block for the synthesis of pharmaceuticals due to its potential applications in medicinal chemistry. It may serve as a precursor or intermediate in the development of new drugs, contributing to the creation of innovative treatments and medications.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 1H-Pyrrolizine-7a(5H)-carboxylic acid, tetrahydro-3-oxo-, phenylmethyl ester is used as a chemical intermediate. This allows for its incorporation into the manufacture of various organic compounds, expanding its utility beyond the pharmaceutical sector.
Used in Industrial Applications:
1H-Pyrrolizine-7a(5H)-carboxylic acid, tetrahydro-3-oxo-, phenylmethyl ester may also have industrial applications as a chemical intermediate in the production of different products. Its versatility in synthesis makes it a valuable component in various industrial processes.
Safety Precautions:
Due to its potential reactivity and toxicity, it is crucial to handle 1H-Pyrrolizine-7a(5H)-carboxylic acid, tetrahydro-3-oxo-, phenylmethyl ester with proper safety measures. This includes the use of personal protective equipment, working in well-ventilated areas, and adhering to established safety protocols to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 216392-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,3,9 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 216392-65:
(8*2)+(7*1)+(6*6)+(5*3)+(4*9)+(3*2)+(2*6)+(1*5)=133
133 % 10 = 3
So 216392-65-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H17NO3/c17-13-7-9-15(8-4-10-16(13)15)14(18)19-11-12-5-2-1-3-6-12/h1-3,5-6H,4,7-11H2
216392-65-3Relevant articles and documents
Intramolecular catalysis of amide isomerization: Kinetic consequences of the 5-NH- -N(a) hydrogen bond in prolyl peptides
Cox, Christopher,Lectka, Thomas
, p. 10660 - 10668 (2007/10/03)
The presence of an intramolecular hydrogen bond has been proposed to play a key role in the catalysis of amide isomerization by peptidylprolyl isomerases (PPIases), which are highly conserved and ubiquitous rotamase enzymes that catalyze the cis-trans iso
