2412-97-7 Usage
General Description
3,5-Dichloro-2,4,6-trimethoxypyridine is a chemical compound with the molecular formula C8H10Cl2N2O3. It is a derivative of pyridine and contains three methoxy groups and two chlorine atoms attached to the pyridine ring. 3,5-Dichloro-2,4,6-trimethoxypyridine is used in organic synthesis as a building block for various pharmaceutical and agrochemical products. It is also used as an intermediate in the production of other chemicals, and its unique structural properties make it valuable in the development of new materials and substances. The compound's specific properties and reactivity make it a useful tool in chemical research and development, and it is considered a valuable asset in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 2412-97-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2412-97:
(6*2)+(5*4)+(4*1)+(3*2)+(2*9)+(1*7)=67
67 % 10 = 7
So 2412-97-7 is a valid CAS Registry Number.
2412-97-7Relevant articles and documents
Synthesis of new pyridines with oligocations and oxygen nucleophiles.
Schmidt, Andreas,Mordhorst, Thorsten,Habeck, Tobias
, p. 1375 - 1377 (2002)
Nucleophilic substitution of 4-(dimethylamino)pyridine on pentachloropyridine yielded pentakis(pyridine-2,3,4,5,6-pentayl)pyridinium, tris-(3,5-dichloropyridine-2,4,6-triyl)pyridinium, or (tetrachloropyridin-4-yl)pyridinium depending on the reaction conditions. Nucleophilic substitution with water, hydroxides, and alcoholates resulted in new betaines and highly substituted pyridines. [structure: see text]
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Moshchitskii,S.D. et al.
, (1975)
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Synthesis of alkoxy-substituted pyridines from mono- and tricationic pyridinium salts
Schmidt, Andreas,Mordhorst, Thorsten
, p. 781 - 786 (2007/10/03)
Nucleophilic substitution reactions on 4-(4-dimethyl-amino)-pyridinium- substituted tetrachloropyridine with oxygen nucleophiles such as alkoxides and phenolates resulted in the formation of 4- or 2,4-alkoxy- or -phenoxy-substituted chloropyridines depend
