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1351611-14-7

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1351611-14-7 Usage

Description

N-formyl 1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxo-1-piperidinyl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazole-[3,4-c]pyridine-3-carboxamide is a complex organic compound with a unique molecular structure. It is derived from Apixaban, a potent and selective inhibitor of coagulation factor Xa, which plays a crucial role in the blood clotting process. N-formyl 1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxo-1-piperidinyl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazole-[3,4-c]pyridine-3-carboxamide exhibits potential therapeutic properties and may be utilized in various medical applications.

Uses

Used in Pharmaceutical Industry:
N-formyl 1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxo-1-piperidinyl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazole-[3,4-c]pyridine-3-carboxamide is used as a potential new oral coagulant for the prevention of venous thromboembolism. It is particularly useful in total hip and knee replacement orthopedic surgeries, where the risk of blood clot formation is high.
Used in Cardiology:
In the field of cardiology, N-formyl 1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxo-1-piperidinyl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazole-[3,4-c]pyridine-3-carboxamide is used for the treatment of patients with venous thromboembolic disorder or atrial fibrillation. Its ability to inhibit coagulation factor Xa makes it a valuable asset in managing and preventing stroke and other cardiovascular complications.
Used in Research and Development:
N-formyl 1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxo-1-piperidinyl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazole-[3,4-c]pyridine-3-carboxamide is also utilized in research and development for the discovery of novel therapeutic agents targeting coagulation pathways. Its unique structure and properties make it an interesting candidate for further investigation and potential development into new drugs for various medical conditions related to blood clotting and cardiovascular health.

Check Digit Verification of cas no

The CAS Registry Mumber 1351611-14-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,1,6,1 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1351611-14:
(9*1)+(8*3)+(7*5)+(6*1)+(5*6)+(4*1)+(3*1)+(2*1)+(1*4)=117
117 % 10 = 7
So 1351611-14-7 is a valid CAS Registry Number.

1351611-14-7Downstream Products

1351611-14-7Relevant articles and documents

A mechanistic study on the amidation of esters mediated by sodium formamide

Ramirez, Antonio,Mudryk, Boguslaw,Rossano, Lucius,Tummala, Srinivas

experimental part, p. 775 - 779 (2012/03/11)

Kinetic and computational studies on the amidation of esters with mixtures of formamide and sodium methoxide are described. Rate studies are consistent with a fast deprotonation of formamide followed by two reversible acyl transfers affected by solvent pa

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