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2-(2,4-dimethyl-phenyl)-4H-isoquinoline-1,3-dione is a complex organic chemical compound with the molecular formula C17H13NO2. It is characterized by a 4H-isoquinoline core, which is a heterocyclic aromatic ring system consisting of two benzene rings fused to a pyridine ring. The compound features a 2,4-dimethylphenyl group attached to the isoquinoline core, which contributes to its unique chemical properties. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its structural diversity and reactivity. It is also of interest in the field of organic chemistry for its potential use as a building block in the creation of more complex molecules.

20863-86-9

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20863-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20863-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,6 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20863-86:
(7*2)+(6*0)+(5*8)+(4*6)+(3*3)+(2*8)+(1*6)=109
109 % 10 = 9
So 20863-86-9 is a valid CAS Registry Number.

20863-86-9Downstream Products

20863-86-9Relevant academic research and scientific papers

Phenylhomophthalimide-type NOS inhibitors derived from thalidomide

Noguchi, Tomomi,Sano, Hiroko,Shimazawa, Rumiko,Tanatani, Aya,Miyachi, Hiroyuki,Hashimoto, Yuichi

, p. 4141 - 4145 (2004)

Thalidomide shows moderate inhibitory activity toward neuronal nitric oxide synthase (nNOS) and inducible NOS (iNOS), but not toward endothelial NOS (eNOS). Structural development studies of thalidomide yielded novel phenylhomophthalimide-type NOS inhibitors with enhanced activity and different subtype selectivity.

Specific inhibitor of puromycin-sensitive aminopeptidase with a homophthalimide skeleton: Identification of the target molecule and a structure-activity relationship study

Komoda, Masato,Kakuta, Hiroki,Takahashi, Hiroyasu,Fujimoto, Yasuyuki,Kadoya, Shizuo,Kato, Fuminori,Hashimoto, Yuichi

, p. 121 - 131 (2007/10/03)

2-(2,6-Diethylphenyl)-1,2,3,4-tetrahydroisoquinoline-1,3-dione (2: PIQ-22) was found to be a potent and specific inhibitor of puromycin-sensitive aminopeptidase (PSA). Lineweaver-Burk plot analysis showed that PSA is inhibited by PIQ-22 in a non-competitive manner. Structure-activity relationship studies indicated that tautomerism of the imidobenzoylketone group in the cyclic imide moiety of the PIQ-22 skeleton is important for the inhibitory activity.

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