123506-67-2 Usage
Uses
Used in Pharmaceutical Synthesis:
3-Pyridinecarboxaldehyde, 6-methoxy-5-methyl(9CI) is used as a key intermediate in the production of various pharmaceuticals. Its unique structure allows it to be a versatile building block in the development of new drugs with potential therapeutic applications.
Used in Research:
3-Pyridinecarboxaldehyde, 6-methoxy-5-methyl(9CI) is also utilized in research settings to study its pharmacological properties. It has been investigated for its role as a cholinergic antagonist, which could have implications for the treatment of neurological disorders.
Used in Anti-Inflammatory Applications:
3-Pyridinecarboxaldehyde, 6-methoxy-5-methyl(9CI) has shown potential as an anti-inflammatory agent. Its use in this capacity could lead to the development of new treatments for inflammatory conditions, offering an alternative to existing medications.
Used in Organic Chemistry:
As an intermediate in the production of other chemical compounds, 3-Pyridinecarboxaldehyde, 6-methoxy-5-methyl(9CI) plays a significant role in the field of organic chemistry. Its ability to be modified and incorporated into a wide range of molecules makes it an important component in chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 123506-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,5,0 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123506-67:
(8*1)+(7*2)+(6*3)+(5*5)+(4*0)+(3*6)+(2*6)+(1*7)=102
102 % 10 = 2
So 123506-67-2 is a valid CAS Registry Number.
123506-67-2Relevant academic research and scientific papers
Lithiation of Methoxypyridines Directed by α-Amino Alkoxides
Comins, Daniel L.,Killpack, Michael O.
, p. 69 - 73 (2007/10/02)
The addition of methoxypyridinecarboxaldehydes to certain lithium dialkylamides gave α-amino alkoxides in situ that were ring-lithiated with alkyllithium bases.Alkylation and hydrolysis on workup provided ring-substituted methoxypyridinecarboxaldehydes via a one-pot reaction.The one-pot methylation of isomeric methoxypyridinecarboxaldehydes was examined.The regioselectivity of the lithiation-methylation was dependent on the aldehyde, the amine component of the α-amino alkoxide, and the metalation conditions.When lithiated N,N,N'-trimethylethylenediamine was used as the amine component of the α-amino alkoxide, methylation generally occured ortho to the aldehyde function.The analogous reactions using lithium N-methylpiperazide as the amine component gave substitution next to the methoxy group.Several new methylated methoxypyridinecarboxaldehydes were prepared in a regioselective manner by using this one-pot procedure.
