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N-(2-methyl-4-amino-5-pyrimidinyl)methylaniline is a chemical compound with the molecular formula C12H15N5. It is an organic molecule that features a pyrimidine ring system, which is a common structural motif in various biologically active compounds. The compound is characterized by a methyl group attached to the pyrimidine core, an amino group at the 4-position, and a methylaniline group connected through a methylene bridge. This specific arrangement of functional groups may confer unique chemical and biological properties, making it a potential candidate for further study in pharmaceutical or chemical research. The compound's structure and potential applications could be of interest to scientists exploring new drug candidates or materials with specific reactivity profiles.

1886-29-9

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1886-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1886-29-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1886-29:
(6*1)+(5*8)+(4*8)+(3*6)+(2*2)+(1*9)=109
109 % 10 = 9
So 1886-29-9 is a valid CAS Registry Number.

1886-29-9Relevant academic research and scientific papers

Thiamine Biosynthesis in Yeast - Evaluation of 4-Hydroxy-5-hydroxymethyl-2-methylpyrimidine as a Precursor

Baxter, Robert L.,Hanley, A. Bryan,Chan, Henry W. S.

, p. 2963 - 2966 (1990)

The putative role of 4-hydroxy-5-hydroxymethyl-2-methylpyrimidine 2 as a late precursor in the biosynthesis of thiamine 1 by Saccharomyces cerevisiae has been examined using the deuteriated derivative 2a.To enable measurement of deuterium incorporation into the pyrimidine ring fragment of 1, a procedure for the degradation of 1 to the aniline derivative 6 using thiaminase I from Bacillus thiaminolyticus has been developed.While 4-amino-2-methyl-5-hydroxymethylpyrimidine 3a was incorporated into thiamine, deuterium from hydroxy-pyrimidine 2a was not incorporated to any significant extent, indicating that amination of compound 2 is not a late step in the biosynthesis of the pyrimidine ring.

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