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
This compound 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 this compound.
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.
