876492-00-1 Usage
General Description
4-Iodo-6-methoxyquinoline is a chemical compound with the molecular formula C10H8INO2. It is a synthetic compound that is used in various research and industrial applications. It is a quinoline derivative with a methoxy group at the 6-position and an iodo substitution at the 4-position. 4-IODO-6-METHOXYQUINOLINE has potential applications in the synthesis of pharmaceuticals, as well as in organic chemistry research. It is also used as a building block for the development of new chemical compounds with potential biological or industrial properties. Additionally, 4-iodo-6-methoxyquinoline has been studied for its antimicrobial and anti-inflammatory properties, making it a potentially valuable chemical for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 876492-00-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,4,9 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 876492-00:
(8*8)+(7*7)+(6*6)+(5*4)+(4*9)+(3*2)+(2*0)+(1*0)=211
211 % 10 = 1
So 876492-00-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H8INO/c1-13-7-2-3-10-8(6-7)9(11)4-5-12-10/h2-6H,1H3
876492-00-1Relevant articles and documents
Microwave-assisted trans-halogenation reactions of various chloro-, bromo-, trifluoromethanesulfonyloxy- and nonafluorobutanesulfonyloxy-substituted quinolines, isoquinolines, and pyridines leading to the corresponding iodinated heterocycles
Bissember, Alex C.,Banwell, Martin G.
supporting information; experimental part, p. 4893 - 4895 (2009/10/02)
(Chemical Equation Presented) Microwave irradiation of certain chloro-, bromo-, trifluoromethanesulfonyloxy- and nonafluorobutanesulfonyloxy-substituted quinolines in the presence of acetic anhydride and sodium iodide leads, via a trans-halogenation process, to the corresponding iodides in high yield. Related conversions involving pyridines and isoquinolines can also be achieved under similar conditions.
