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5623-92-7

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  • 2-[8-oxo-4-(trifluoromethyl)-10-thia-7-azabicyclo[4.4.0]deca-2,4,11-trien-9-yl]-N-(2-propoxyphenyl)acetamide

    Cas No: 5623-92-7

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5623-92-7 Usage

Molecular Weight

144.22 g/mol
The mass of one mole of 1-piperazinebutanol.

Physical Appearance

White Crystalline Solid
A solid with a white, crystalline appearance.

Synthesis

Pharmaceutical Applications
Used in the creation of various pharmaceuticals, such as anti-arrhythmic and anti-histaminic drugs.

Industrial Uses

Corrosion Inhibitor and Surfactant Manufacturing
Acts as a corrosion inhibitor in various materials and is used in the production of certain surfactants.

Stability

High
Known for its high stability in different conditions.

Toxicity

Low
Exhibits low toxicity, making it a valuable component in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5623-92-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5623-92:
(6*5)+(5*6)+(4*2)+(3*3)+(2*9)+(1*2)=97
97 % 10 = 7
So 5623-92-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H19F3N2O3S/c1-2-9-28-15-6-4-3-5-13(15)24-18(26)11-17-19(27)25-14-10-12(20(21,22)23)7-8-16(14)29-17/h3-8,10,17H,2,9,11H2,1H3,(H,24,26)(H,25,27)

5623-92-7Relevant articles and documents

Design and synthesis of novel sulfonamide-containing bradykinin hB 2 receptor antagonists. Synthesis and structure-relationships of α,α-tetrahydropyranylglycine

Fincham, Christopher I.,Bressan, Alessandro,D'Andrea, Piero,Ettorre, Alessandro,Giuliani, Sandro,Mauro, Sandro,Meini, Stefania,Paris, Marielle,Quartara, Laura,Rossi, Cristina,Squarcia, Antonella,Valenti, Claudio,Daniela, Fattori,Maggi, Carlo Alberto

supporting information; experimental part, p. 2091 - 2100 (2012/05/05)

A series of α,α-cycloalkylglycine sulfonamide compounds of general formula 1 has previously been identified by our group as selective human B2(hB2) receptor antagonists. Here we report the in vitro and in vivo BK antagonist activity

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