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Pyrimidine, 5-methoxy-4-methyl(8CI,9CI) is a chemical compound with the molecular formula C7H8N2O. It is a derivative of pyrimidine, which is a heterocyclic aromatic organic compound that contains nitrogen. The 5-methoxy-4-methyl substitution in Pyrimidine, 5-methoxy-4-methyl- (8CI,9CI) gives it unique chemical and biological properties. It may have potential applications in pharmaceuticals, as well as in the field of organic synthesis. Its precise uses and effects have not been widely studied or documented, but it is of interest to researchers due to its structural characteristics and potential for novel chemical reactivity.

19175-07-6

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19175-07-6 Usage

Uses

Used in Pharmaceutical Industry:
Pyrimidine, 5-methoxy-4-methyl(8CI,9CI) is used as a pharmaceutical compound for its potential therapeutic applications. Its unique chemical and biological properties make it a promising candidate for the development of new drugs and treatments.
Used in Organic Synthesis:
Pyrimidine, 5-methoxy-4-methyl(8CI,9CI) is used as a building block in organic synthesis for the creation of more complex molecules. Its structural characteristics and potential for novel chemical reactivity make it a valuable component in the synthesis of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 19175-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,7 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19175-07:
(7*1)+(6*9)+(5*1)+(4*7)+(3*5)+(2*0)+(1*7)=116
116 % 10 = 6
So 19175-07-6 is a valid CAS Registry Number.

19175-07-6Relevant academic research and scientific papers

Studies on Pyrimidine Derivatives. XXXIX. Site-Selectivity in the Reaction of 5-Substituted and 4,5-Disubstituted Pyrimidine N-Oxides with Trimethylsilyl Cynanide

Yamanaka, Hiroshi,Sakamoto, Takao,Nishimura, Sumiko,Sagi, Mataichi

, p. 3119 - 3126 (2007/10/02)

The site-selectivity in the modified Reissert-Henze reaction of 5-substituted and 4,5-disubstituted pyrimidine 1-oxides with trimethylsilyl cyanide was examined.The reaction of 5-substituted 4-methoxypyrimidine 1-oxides with trimethylsilyl cyanide gave exclusively 2-pyrimidinecarbonitriles in good yields without exception.On the other hand, the other 5-substituted and 4,5-disubstituted pyrimidine 1-oxides gave mainly 6-pyrimidinecarbonitriles.Keywords--site-selectivity; pyrimidine N-oxide; trimethylsilyl cyanide; Reissert-Henze reasction; pyrimidinecarbonitrile

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