101624-26-4 Usage
Molecular Structure
2-(4-Methoxyphenyl)indolizine-3-carboxaldehyde is an indolizine derivative with a 2-(4-methoxyphenyl) substituent and a carboxaldehyde group at position 3 of the ring.
Chemical Class
It belongs to the class of indolizine derivatives.
Substituent
The compound has a 2-(4-methoxyphenyl) substituent on the indolizine ring.
Functional Group
The compound has a carboxaldehyde group at position 3 of the ring.
Pharmacological Properties
2-(4-Methoxyphenyl)indolizine-3-carboxaldehyde has interesting pharmacological properties, such as its ability to act as an inhibitor of specific biological targets.
Potential Applications
The compound has potential applications in medicinal chemistry and drug discovery due to its pharmacological properties.
Implications
Further research and development in this area could lead to the discovery of new therapeutic agents with possible implications for the treatment of various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 101624-26-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,6,2 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 101624-26:
(8*1)+(7*0)+(6*1)+(5*6)+(4*2)+(3*4)+(2*2)+(1*6)=74
74 % 10 = 4
So 101624-26-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H13NO2/c1-19-14-7-5-12(6-8-14)15-10-13-4-2-3-9-17(13)16(15)11-18/h2-11H,1H3
101624-26-4Relevant articles and documents
Direct positive dyes made from 3-indolizine carboxaldehyde
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, (2008/06/13)
A new group of cyanine and merocyanine spectral sensitizing dyes based on derivatives of 3-indolizine carboxaldehyde is particularly useful in sensitizing a direct positive silver halide emulsion to orange and red.
