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2-phenylamino-3-amino-6-methoxypyridine is a complex organic compound with the molecular formula C12H13N3O. It features a pyridine ring, which is a six-membered aromatic ring containing two nitrogen atoms, with a phenyl group (C6H5) attached to the 2-position, an amino group (NH2) at the 3-position, and a methoxy group (OCH3) at the 6-position. 2-phenylamino-3-amino-6-methoxypyridine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through multi-step organic reactions and is used as an intermediate in the preparation of more complex molecules. The compound's properties, such as its solubility and stability, can be influenced by the presence of the phenyl, amino, and methoxy groups, making it a versatile building block in organic chemistry.

6604-51-9

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6604-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6604-51-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,0 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6604-51:
(6*6)+(5*6)+(4*0)+(3*4)+(2*5)+(1*1)=89
89 % 10 = 9
So 6604-51-9 is a valid CAS Registry Number.

6604-51-9Upstream product

6604-51-9Relevant academic research and scientific papers

Design and synthesis of novel benzimidazole derivatives as phosphodiesterase 10A inhibitors with reduced CYP1A2 inhibition

Hamaguchi, Wataru,Masuda, Naoyuki,Isomura, Mai,Miyamoto, Satoshi,Kikuchi, Shigetoshi,Amano, Yasushi,Honbou, Kazuya,Mihara, Takuma,Watanabe, Toshihiro

, p. 7612 - 7623 (2013)

A novel class of phosphodiesterase 10A (PDE10A) inhibitors with reduced CYP1A2 inhibition were designed and synthesized starting from 2-{[(1-phenyl-1H-benzimidazol-6-yl)oxy]methyl}quinoline (1). Introduction of an isopropyl group at the 2-position and a methoxy group at the 5-position of the benzimidazole ring of lead compound 1 resulted in the identification of 2-{[(2-isopropyl-5-methoxy-1-phenyl-1H-benzimidazol-6-yl)oxy]methyl}quinoline (25b), which exhibited potent PDE10A inhibitory activity with reduced CYP1A2 inhibitory activity compared to compound 1.

Imidazopyridine derivatives as PI3K inhibitors

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Page/Page column 35, (2012/11/13)

New imidazopyridine derivatives having the chemical structure of formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Phosphoinositide 3-Kinases (PI3Ks)

IMIDAZOPYRIDINE DERIVATIVES AS PI3K INHIBITORS

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Page/Page column 84, (2012/11/13)

New imidazopyridine derivatives having the chemical structure of formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Phosphoinositide 3-Kinases (PI3Ks).

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