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1-phenethyl-1H-pyrrole-2-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

49795-42-8

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49795-42-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49795-42-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,7,9 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 49795-42:
(7*4)+(6*9)+(5*7)+(4*9)+(3*5)+(2*4)+(1*2)=178
178 % 10 = 8
So 49795-42-8 is a valid CAS Registry Number.

49795-42-8Relevant academic research and scientific papers

A three-residue, continuous binding epitope peptidomimetic of ShK toxin as a Kv1.3 inhibitor

Harvey, Andrew J.,Gable, Robert W.,Baell, Jonathan B.

, p. 3193 - 3196 (2005)

The ShK toxin is a polypeptide that blocks the Kv1.3 potassium channel in T-lymphocytes and has been identified as a potential therapeutic for multiple sclerosis. ShK is well characterised in terms of structure and binding, offering an attractive target for the design of structural and functional mimetics. Building on our previous success in developing rationally designed peptidomimetics of ShK, we report a novel mimetic of the K22-Y23-R24 residues of the peptide. The mimetic was shown to inhibit the Kv1.3 channel with moderate activity.

Selective and Efficient Formylation of Indoles (C3) and Pyrroles (C2) Using 2,4,6-Trichloro-1,3,5-Triazine/Dimethylformamide (TCT/DMF) Mixed Reagent

Iranpoor, Nasser,Panahi, Farhad,Erfan, Soodabeh,Roozbin, Fatemeh

, p. 904 - 910 (2017/03/27)

This study introduces an efficient method for the selective formylation of indoles and pyrroles at the positions of C(3) and C(2), respectively. The mixture of three equivalents of N,N-dimethylformamide and one equivalent of 2,4,6-trichloro-1,3,5-triazine (cyanuric chloride) generates an easy handling formylating agent for the efficient formylation of these classes of compounds to give the corresponding aldehydes under mild reaction conditions. This procedure was highly efficient, and a range of formylated indoles and pyrroles were obtained in good to excellent yields.

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