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340774-26-7

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340774-26-7 Usage

Description

(1-cyclopropyl-methanoyl)-dimethylamino-acrylic acid methyl ester, also known as 2-Cyclopropylcarbonyl-3-dimethylaminoacrylic Acid Methyl Ester, is an organic compound that serves as a crucial intermediate in the synthesis of pharmaceuticals. It is characterized by its unique molecular structure, which includes a cyclopropylcarbonyl group, a dimethylamino group, and a methyl ester group attached to an acrylic acid backbone. (1-cyclopropyl-methanoyl)-dimethylamino-acrylic acid methyl ester plays a significant role in the development of soluble guanylyl cyclase activators, which are important in the treatment of various medical conditions.

Uses

Used in Pharmaceutical Industry:
(1-cyclopropyl-methanoyl)-dimethylamino-acrylic acid methyl ester is used as an intermediate in the synthesis of soluble guanylyl cyclase activators for the treatment of medical conditions such as pulmonary arterial hypertension, heart failure, and certain types of anemia. Its role in the synthesis process is to provide a structural foundation for the development of these activators, which can modulate the activity of guanylyl cyclase, a key enzyme in the regulation of vascular tone and blood flow.

Check Digit Verification of cas no

The CAS Registry Mumber 340774-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,0,7,7 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 340774-26:
(8*3)+(7*4)+(6*0)+(5*7)+(4*7)+(3*4)+(2*2)+(1*6)=137
137 % 10 = 7
So 340774-26-7 is a valid CAS Registry Number.

340774-26-7Relevant articles and documents

PLASMA KALLIKREIN INHIBITORS

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Page/Page column 48-49, (2022/04/03)

The present invention provides a compound of Formula (I) and pharmaceutical compositions comprising one or more said compounds, and methods for using said compounds for treating or preventing one or more disease states that could benefit from inhibition of plasma kallikrein, including hereditary angioedema, uveitis, posterior uveitis, wet age related macular edema, diabetic macular edema, diabetic retinopathy and retinal vein occlusion. The compounds are selective inhibitors of plasma kallikrein.

METHOD FOR PRODUCING PYRROLIDINE COMPOUND

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Page/Page column 93, (2009/10/01)

Provided is a method capable of efficiently producing a compound having a superior HSD1 inhibitory action and a compound useful as a synthetic intermediate therefor, with superior achievability of asymmetric synthesis (i.e., superior selectivity), superior yield, superior safety and superior industrial workability at a low cost. A method of producing a compound represented by the following formula [8]: or a salt thereof, or a solvate thereof, from a compound represented by the following formula [2]: or a reactive derivative thereof, or a salt thereof, or a solvate thereof.

3-‘4-HETEROCYCLYL -1,2,3,-TRIAZOL-1-YL!-N-ARYL-BENZAMIDES AS INHIBITORS OF THE CYTOKINES PRODUCTION FOR THE TREATMENT OF CHRONIC INFLAMMATORY DISEASES

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Page/Page column 99, (2008/06/13)

Disclosed compounds of formula (I), which inhibit production of cytokines involved in inflammatory processes and are thus useful for treating diseases and pathological conditions involving inflammation such as chronic inflammatory disease. Also disclosed are processes for preparing these compounds and pharmaceutical compositions comprising these compounds.

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