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6-(methoxymethyl)-2-methylpyrimidin-4(1H)-one is a heterocyclic organic compound characterized by a pyrimidin-4(1H)-one core structure, which features a pyrimidine ring with a carbonyl group at position 4 and a hydrogen atom at position 1. 6-(methoxymethyl)-2-methylpyrimidin-4(1H)-one is further distinguished by the presence of a methyl group at the 2-position and a methoxymethyl group at the 6-position. The methoxymethyl group is an ether derivative of a methyl group, where the hydrogen atom is replaced by a methoxy group (-OCH3). This chemical structure may be relevant in various applications, such as pharmaceuticals or chemical research, due to its potential reactivity and the ability to form derivatives. The compound's specific properties, such as solubility, stability, and reactivity, can be influenced by the presence of these functional groups, making it a subject of interest for synthetic chemists and researchers in related fields.

3122-75-6

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3122-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3122-75-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,2 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3122-75:
(6*3)+(5*1)+(4*2)+(3*2)+(2*7)+(1*5)=56
56 % 10 = 6
So 3122-75-6 is a valid CAS Registry Number.

3122-75-6Relevant academic research and scientific papers

Studies on Pyrimidine Derivatives. XXXII. Reaction of 4-Substituted 2,6-Dimethylpyrimidine 1-Oxides with Phosphoryl Chloride

Sakamoto, Takao,Yoshizawa, Hiroshi,Kaneda, Sohichi,Hama, Yoshiaki,Yamanaka, Hiroshi

, p. 4533 - 4538 (2007/10/02)

The reaction of 2,6-dimethyl-4-phenylpyrimidine 1-oxide with phosphoryl chloride gave 4-chloromethyl-2-methyl-6-phenylpyrimidine exclusively.In contrast, 2,6-dimethyl-4-methoxy-pyrimidine 1-oxide and 2,6-dimethyl-4-dimethylaminopyrimidine 1-oxide reacted with the same reagent to give the corresponding 2-chloromethylpyrimidines predominantly.Keywords - pyrimidine N-oxide; chloromethylpyrimidine; phosphoryl chloride; siteselective reaction; substituent effect

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