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4-amino-5-bromo-2,6-dimethoxypyrimidine is a heterocyclic organic compound characterized by a pyrimidine ring structure, which is a six-membered aromatic ring containing four carbon atoms and two nitrogen atoms. This specific compound features a bromine atom at the 5-position, an amino group at the 4-position, and two methoxy groups at the 2 and 6 positions. The presence of these functional groups endows the molecule with unique chemical properties and reactivity, making it a potentially valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals. The bromine atom can be used for further functionalization, while the amino group can participate in a range of reactions, such as acylation or alkylation. The methoxy groups can influence the molecule's solubility and reactivity, and may also be replaced with other functional groups through chemical transformations. Overall, 4-amino-5-bromo-2,6-dimethoxypyrimidine is a versatile building block in organic synthesis, with potential applications in the development of new drugs and other chemical products.

6584-20-9

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6584-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6584-20-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,8 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6584-20:
(6*6)+(5*5)+(4*8)+(3*4)+(2*2)+(1*0)=109
109 % 10 = 9
So 6584-20-9 is a valid CAS Registry Number.

6584-20-9Relevant academic research and scientific papers

Condensed heteroaromatic ring systems. XXI. Synthesis of pyrrolo[2,3-d]pyrimidines and pyrrolo[3,2-d]pyrimidines

Sakamoto,Satoh,Kondo,Yamanaka

, p. 81 - 86 (2007/10/02)

Pyrrolo[2,3-d]pyrimidines and pyrrolo[3,2-d]pyrimidines were synthesized in high yields by the palladium-catalyzed reaction of 4-acetylamino-5-bromopyrimidines and 5-acetylamino-4-iodopyrimidines with (Z)-1-ethoxy-2-(tributylstannyl)ethene followed by cyclization under acidic conditions.

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