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2-Thiophenesulfonamide, 3-[4-[(2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridin-3-yl)methyl]phenyl]- 5-(2-methylpropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

151467-40-2

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151467-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151467-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,4,6 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 151467-40:
(8*1)+(7*5)+(6*1)+(5*4)+(4*6)+(3*7)+(2*4)+(1*0)=122
122 % 10 = 2
So 151467-40-2 is a valid CAS Registry Number.

151467-40-2Downstream Products

151467-40-2Relevant academic research and scientific papers

Scandium triflate as an efficient and recyclable catalyst for the deprotection of tert-butyl aryl sulfonamides

Mahalingam,Wu, Xiongyu,Wan, Yiqian,Alterman, Mathias

, p. 417 - 425 (2007/10/03)

A mild and efficient method for deprotection of tert-butyl sulfonamide groups utilizing Sc(OTf)3 as deprotecting reagent has been developed. A variety of tert-butyl aryl sulfonamides used under these conditions gave the corresponding primary sulfonamides in high yields. The Lewis acid catalyst could be fully recovered and reused with maintained activity after the reactions. Copyright Taylor & Francis, Inc.

First Reported Nonpeptide AT1 Receptor Agonist (L-162,313) Acts as an AT2 Receptor Agonist in Vivo

Wan, Yiqian,Wallinder, Charlotta,Johansson, Berndt,Holm, Mathias,Mahalingam,Wu, Xiongyu,Botros, Milad,Karlén, Anders,Pettersson, Anders,Nyberg, Fred,F?ndriks, Lars,Hallberg, Anders,Alterman, Mathias

, p. 1536 - 1546 (2007/10/03)

In this investigation, it is demonstrated that the first nonpeptide AT 1 receptor agonist L-162,313 (1), disclosed in 1994, also acts as an agonist at the AT2 receptor. In anesthetized rats, administration of compound 1 intravenously

Boron trichloride as an efficient and selective agent for deprotection of tert-butyl aryl sulfonamides

Wan, Yiqian,Wu, Xiongyu,Kannan, Mahalingam A.,Alterman, Mathias

, p. 4523 - 4525 (2007/10/03)

A fast, mild and selective method for deprotection of tert-butyl aryl sulfonamides utilizing BCl3 as deprotection reagent has been developed. A variety of tert-butyl aryl sulfonamides used under these conditions gave the corresponding primary sulfonamides in high yields. The method does not cleave methoxy groups and prevents incorporation of tert-butyl groups onto electron-rich aromatic rings.

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