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[3-(1-{4-[2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-benzenesulfonylamino]-tetrahydro-pyran-4-carbonyl}-piperidin-4-yl)-propyl]-trimethyl-ammonium trilfuoroacetate salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1369390-39-5

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  • [3-(1-{4-[2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-benzenesulfonylamino]-tetrahydro-pyran-4-carbonyl}-piperidin-4-yl)-propyl]-trimethyl-ammonium trilfuoroacetate salt

    Cas No: 1369390-39-5

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  • Jiangsu Congzhong Chemical Co., Ltd.
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  • [3-(1-{4-[2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-benzenesulfonylamino]-tetrahydro-pyran-4-carbonyl}-piperidin-4-yl)-propyl]-trimethyl-ammonium trilfuoroacetate salt

    Cas No: 1369390-39-5

  • Need to discuss

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  • Jiangsu King Road New Materials Co., Ltd.
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1369390-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1369390-39-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,9,3,9 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1369390-39:
(9*1)+(8*3)+(7*6)+(6*9)+(5*3)+(4*9)+(3*0)+(2*3)+(1*9)=195
195 % 10 = 5
So 1369390-39-5 is a valid CAS Registry Number.

1369390-39-5Downstream Products

1369390-39-5Relevant 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

, 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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