38749-96-1 Usage
Description
Pyridine, 3-iodo-4-methyl(9CI) is an organic compound that belongs to the pyridine family. It is characterized by the presence of an iodine atom at the 3-position and a methyl group at the 4-position on the pyridine ring. Pyridine, 3-iodo-4-methyl(9CI) is known for its unique chemical properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
Pyridine, 3-iodo-4-methyl(9CI) is used as a reactant in the preparation of 7a-heteroarylhexahydro-1H-pyrrolizines. These compounds act as cholinergic synaptic transmission modulators, which are important in the treatment of neurological disorders and cognitive functions. The introduction of the iodine and methyl groups in the pyridine ring provides specific structural features that contribute to the modulation of cholinergic synaptic transmission.
Check Digit Verification of cas no
The CAS Registry Mumber 38749-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,4 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38749-96:
(7*3)+(6*8)+(5*7)+(4*4)+(3*9)+(2*9)+(1*6)=171
171 % 10 = 1
So 38749-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H6IN/c1-5-2-3-8-4-6(5)7/h2-4H,1H3
38749-96-1Relevant articles and documents
Anti-Markovnikov Hydroarylation of Unactivated Olefins via Pyridyl Radical Intermediates
Boyington, Allyson J.,Riu, Martin-Louis Y.,Jui, Nathan T.
supporting information, p. 6582 - 6585 (2017/05/29)
The intermolecular alkylation of pyridine units with simple alkenes has been achieved via a photoredox radical mechanism. This process occurs with complete regiocontrol, where single-electron reduction of halogenated pyridines regiospecifically yields the corresponding radicals in a programmed fashion, and radical addition to alkene substrates occurs with exclusive anti-Markovnikov selectivity. This system is mild, tolerant of many functional groups, and effective for the preparation of a wide range of complex alkylpyridines.
Preparation of 7a-heteroarylhexahydro-1H-pyrrolizines as cholinergic synaptic transmission modulators.
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, (2008/06/13)
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