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(3-AMINO-4,6-DIMETHYL-FURO[2,3-B]PYRIDIN-2-YL)-PHENYL-METHANONE is a synthetic compound that features a furo[2,3-b]pyridin-2-yl group, an amino group, and a phenyl-methanone moiety. It is utilized in pharmaceutical research and drug development as a potential candidate for treating a range of diseases. (3-AMINO-4,6-DIMETHYL-FURO[2,3-B]PYRIDIN-2-YL)-PHENYL-METHANONE is notable for its potential pharmacological properties, such as its capacity to engage with specific biological targets and alter their activity. Further research is essential to fully explore the medicinal applications of this chemical and its impact on biological systems.

54891-82-6

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54891-82-6 Usage

Uses

Used in Pharmaceutical Research:
(3-AMINO-4,6-DIMETHYL-FURO[2,3-B]PYRIDIN-2-YL)-PHENYL-METHANONE is used as a research compound for investigating its interactions with biological targets, which may lead to the development of new therapeutic agents.
Used in Drug Development:
In the field of drug development, (3-AMINO-4,6-DIMETHYL-FURO[2,3-B]PYRIDIN-2-YL)-PHENYL-METHANONE is used as a potential candidate for the treatment of various diseases, leveraging its ability to modulate the activity of specific biological targets.
Used in Medicinal Chemistry:
(3-AMINO-4,6-DIMETHYL-FURO[2,3-B]PYRIDIN-2-YL)-PHENYL-METHANONE is employed in medicinal chemistry to design and synthesize new molecules with improved pharmacological properties, potentially leading to more effective treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 54891-82-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,9 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54891-82:
(7*5)+(6*4)+(5*8)+(4*9)+(3*1)+(2*8)+(1*2)=156
156 % 10 = 6
So 54891-82-6 is a valid CAS Registry Number.

54891-82-6Downstream Products

54891-82-6Relevant academic research and scientific papers

Discovery and SAR of novel mGluR5 non-competitive antagonists not based on an MPEP chemotype

Rodriguez, Alice L.,Williams, Richard,Zhou, Ya,Lindsley, Stacey R.,Le, Uyen,Grier, Mark D.,David Weaver,Jeffrey Conn,Lindsley, Craig W.

scheme or table, p. 3209 - 3213 (2010/03/31)

This Letter describes the discovery and SAR of three novel series of mGluR5 non-competitive antagonists/negative allosteric modulators (NAMs) not based on manipulation of an MPEP/MTEP chemotype. This work demonstrates fundamentally new mGluR5 NAM chemotypes with submicromolar potencies, and the first example of a mode of pharmacology 'switch' to provide PAMs with a non-MPEP scaffold.

Cathylation of 4,6-dimethyl-2-oxopyridine-3-carbonitrile derivatives leading to the synthesis of furo[2,3-b;4,5-b']dipyridines and novel tricyclic furo[2,3,4-ij][2,7]naphthyridine

Lin, Chyun-Feng,Lin, Yi-Feng,Lo, Yan-Chung,Chen, Kuo-Tung,Su, Tsann-Long

, p. 15 - 26 (2007/10/03)

Cathylation of ethyl 2-(3-cyano-4,6-dimethylpyridine-2-yloxy)acetate afforded a trace amount of new tricyclic furo[2,3,4-ij][2,7]naphthyridine derivative. An attempt was made for an alternate method for the synthesis this new tricyclic ring system. Treatm

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