807320-43-0 Usage
Description
cis-1'-Oxo-spiro[cyclohexane-1,3'(1'H)-furo[3,4-c]pyridine]-4-carboxylic acid is a complex chemical compound characterized by a unique spiro ring system that incorporates both cyclohexane and furo[3,4-c]pyridine moieties. This molecule also features a carboxylic acid functional group and a distinctive cis-1'Oxo configuration, which denotes the positioning of a ketone group within the spiro ring system. The intricate structure and functional groups of this compound suggest potential pharmaceutical or biological activities, although further research and testing are required to fully determine its uses and properties.
Uses
Used in Pharmaceutical Development:
cis-1'-Oxo-spiro[cyclohexane-1,3'(1'H)-furo[3,4-c]pyridine]-4-carboxylic acid is used as a potential pharmaceutical candidate due to its complex structure and functional groups. cis-1'-Oxo-spiro[cyclohexane-1,3'(1'H)-furo[3,4-c]pyridine]-4-carboxylic acid's unique molecular architecture may offer novel interactions with biological targets, making it a subject of interest for the development of new drugs.
Used in Biological Research:
In the field of biological research, cis-1'-Oxo-spiro[cyclohexane-1,3'(1'H)-furo[3,4-c]pyridine]-4-carboxylic acid serves as a valuable tool for studying molecular interactions and the effects of structural modifications on biological activity. Its unique features can provide insights into the design of new bioactive molecules and contribute to the understanding of complex biological processes.
Used in Chemical Synthesis:
cis-1'-Oxo-spiro[cyclohexane-1,3'(1'H)-furo[3,4-c]pyridine]-4-carboxylic acid can be utilized as a key intermediate in the synthesis of other complex organic molecules. Its versatile structure allows for further functionalization and modification, making it a useful building block for the creation of novel compounds with potential applications in various industries.
Used in Material Science:
The unique structural features of cis-1'-Oxo-spiro[cyclohexane-1,3'(1'H)-furo[3,4-c]pyridine]-4-carboxylic acid may also find applications in material science. Its potential use in the development of new materials with specific properties, such as improved stability or selectivity, could be explored through ongoing research and development efforts.
Check Digit Verification of cas no
The CAS Registry Mumber 807320-43-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,7,3,2 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 807320-43:
(8*8)+(7*0)+(6*7)+(5*3)+(4*2)+(3*0)+(2*4)+(1*3)=140
140 % 10 = 0
So 807320-43-0 is a valid CAS Registry Number.
807320-43-0Relevant articles and documents
Practical synthesis of a neuropeptide Y antagonist via stereoselective addition to a ketene
Iida, Takehiko,Satoh, Hiroki,Maeda, Kenji,Yamamoto, Yuhei,Asakawa, Ken-Ichi,Sawada, Naotaka,Wada, Toshihiro,Kadowaki, Chie,Itoh, Takahiro,Mase, Toshiaki,Weissman, Steven A.,Tschaen, Dave,Krska, Shane,Volante
, p. 9222 - 9229 (2005)
The synthesis of neuropeptide Y antagonist 1, currently under clinical investigation for the treatment of obesity, is described. The convergent synthesis from trans-spirolactone carboxylic acid intermediate 2a and aminopyrazole 3 is predicated on a stereo
