97336-42-0 Usage
Molecular Weight
163.22 g/mol The molecular weight is the mass of one mole of the compound, calculated by adding the atomic weights of all the atoms in the molecular formula.
Structure
1H-Pyrrole-2-carboxaldehyde, 3-ethyl-4,5-dimethyl(9CI) The structure of the compound is characterized by a pyrrole ring, a carboxaldehyde functional group, an ethyl group, and two methyl groups attached to the pyrrole ring.
Class
Pyrrole-based compounds 1H-Pyrrole-2-carboxaldehyde, 3-ethyl-4,5-dimethyl- (9CI) belongs to a class of chemical compounds that contain a pyrrole ring, which is a five-membered aromatic ring with four carbon atoms and one nitrogen atom.
Functional Groups
Carboxaldehyde, Ethyl, Methyl The presence of these functional groups contributes to the compound's reactivity and potential applications in organic synthesis.
Potential Applications
Organic synthesis, pharmaceuticals, and agrochemicals Due to its unique structure and functional groups, 1H-Pyrrole-2-carboxaldehyde, 3-ethyl-4,5-dimethyl- (9CI) may be used in the production of various pharmaceuticals and agrochemicals.
Reactivity
Varies with chemical structure and synthesis methods The properties and uses of 1H-Pyrrole-2-carboxaldehyde, 3-ethyl-4,5-dimethyl(9CI) may change depending on its specific chemical structure and the methods used to synthesize it.
Check Digit Verification of cas no
The CAS Registry Mumber 97336-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,3 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 97336-42:
(7*9)+(6*7)+(5*3)+(4*3)+(3*6)+(2*4)+(1*2)=160
160 % 10 = 0
So 97336-42-0 is a valid CAS Registry Number.
97336-42-0Relevant academic research and scientific papers
The Chemistry of Pyrrolic Compounds. LXI Petroporphyrins from the Julia Creek Oil Shale: Further Evidence for the Derivation of Aetiotype Petroporphyrins from Chlorophyll
Clezy, Peter S.,Fookes, Christopher J. R.,Prashar, Jognandan K.
, p. 775 - 786 (2007/10/02)
The synthesis of the porphyrins (2c-j) has been achieved by the oxidative cyclization of appropriately substituted biladienes-ac.The availability of authentic material has allowed the finalization of the structure of a series of aetiotype fossil porphyrins which vary in substitution pattern at positions 3 and 13.All combinations of H, Me and Et at these positions have now been isolated from natural sources.This points to a common precursor, possibly a divinylporphyrin, and strengthens the belief that the chlorophylls are the prime source of the petroporphyrins.A vinyl group, or a close derivative, is found at position 3 of all chlorophylls while fragmentation of the ubiquitous isocyclic ring of the chlorophylls could yield the vinyl group at position 13.
