15400-58-5 Usage
Uses
Used in Pharmaceutical Synthesis:
Methyl 2,4-dimethoxypyrimidine-5-carboxylate is used as an intermediate for the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable building block in the production of functionalized pyrimidine derivatives, which are essential components in the development of new drugs.
Used in Agrochemical Synthesis:
In the agrochemical industry, Methyl 2,4-dimethoxypyrimidine-5-carboxylate is employed as an intermediate in the synthesis of various agrochemicals. Its versatility and reactivity contribute to the development of new and effective compounds for agricultural applications.
Used in Organic Chemistry Research:
Methyl 2,4-dimethoxypyrimidine-5-carboxylate is utilized in research and development laboratories for various organic chemistry applications. Its unique properties and reactivity make it a valuable tool for exploring new chemical reactions and synthesizing novel compounds for various purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 15400-58-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,0 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15400-58:
(7*1)+(6*5)+(5*4)+(4*0)+(3*0)+(2*5)+(1*8)=75
75 % 10 = 5
So 15400-58-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O4/c1-12-6-5(7(11)13-2)4-9-8(10-6)14-3/h4H,1-3H3
15400-58-5Relevant academic research and scientific papers
AZABICYCLO [3. 1. O] HEXYL DERIVATIVES AS MODULATORS OF DOPAMINE D3 RECEPTORS
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Page/Page column 59, (2009/05/29)
The present invention relates to novel compounds of formula (I) or a salt thereof: wherein R1 is a 5-membered heteroaryl group, optionally fused with a 6-membered hetero or carbocycle; such 5 or 11-membered system, may be optionally substituted by 1, 2, 3 or 4 substituents selected from the group consisting of: halogen, cyano, C1-4alkyl, haloC1-4alkyl, C1-4alkoxy, C1-4alkanoyl, haloC1-4alkoxy and SF5, and n is 1 or 2; processes for their preparation, intermediates used in these processes, pharmaceutical compositions containing them and their use in therapy, as modulators of dopamine D3 receptors, e.g. to treat drug dependency, as antipsychotic agents, to treat obsessive compulsive spectrum disorders, or premature ejaculation.
SYNTHESIS OF 5-SUBSTITUTED PYRIMIDINES THROUGH ortho-DIRECTED LITHIATION REACTIONS
Wada, Akimori,Yamamoto, Junpei,Kanatomo, Shoichi
, p. 585 - 589 (2007/10/02)
Treatment of 2- and/or 4-substituted pyrimidine with LiTMP in ether at 0 deg C, followed by guenching with various electrophiles afforded the corresponding 5-substituted pyrimidines.
