471248-30-3 Usage
Molecular structure
A cyclic organic compound with a pyridine ring, two hydroxyl groups attached to the 5th and 6th carbon positions, and a methyl group attached to the 1st carbon position.
Stereochemistry
The molecule has a (5S,6S) designation, indicating the specific spatial arrangement of the hydroxyl groups on the pyridine ring.
Potential applications
2(1H)-Pyridinone,5,6-dihydro-5,6-dihydroxy-1-methyl-,(5S,6S)-(9CI) has potential uses in various fields, including pharmaceuticals, agrochemicals, and industrial chemistry.
Synthesis
It may be utilized as an intermediate in the synthesis of other organic compounds or as a building block for the creation of new molecules with specific properties or biological activities.
Further research
Ongoing research and development may reveal additional uses and potential benefits of 2(1H)-Pyridinone,5,6-dihydro-5,6-dihydroxy-1-methyl-,(5S,6S)-(9CI).
Check Digit Verification of cas no
The CAS Registry Mumber 471248-30-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,1,2,4 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 471248-30:
(8*4)+(7*7)+(6*1)+(5*2)+(4*4)+(3*8)+(2*3)+(1*0)=143
143 % 10 = 3
So 471248-30-3 is a valid CAS Registry Number.
471248-30-3Relevant articles and documents
Dioxygenase-catalyzed cis-dihydroxylation of pyridine-ring systems
Boyd, Derek R.,Sharma, Narain D.,Modyanova, Ludmila V.,Carroll, Jonathan G.,Malone, John F.,Allen, Christopher C.R.,Hamilton, John T.G.,Gibson, David T.,Parales, Rebecca E.,Dalton, Howard
, p. 589 - 600 (2007/10/03)
Toluene dioxygenase-catalyzed dihydroxylation, in the carbocyclic rings of quinoline, 2-chloroquinoline, 2-methoxyquinoline, and 3-bromoquinoline, was found to yield the corresponding enantiopure cis-5,6- and -7,8-dihydrodiol metabolites using whole cells
Dioxygenase-catalysed formation of dihydrodiol metabolites of N-methyl- 2-pyridone
Modyanova, Ludmila,Azerad, Robert
, p. 3865 - 3869 (2007/10/03)
IPTG-induced cells of a recombinant strain of Escherichia coli JM109(DE3)pDTG141 expressing naphthalene dioxygenase from Pseudomonas sp. NCIB 9816-4 oxidized specifically N-methyl-2-pyridone to give the corresponding cis-5,6-dihydro-5,6-dihydroxy derivative as a major product. A small amount of the cis-3,4-dihydro-3,4-dihydroxy isomer was simultaneously formed. (C) 2000 Elsevier Science Ltd.
