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5-Nitro-2-(trichloroacetyl)-1-methylpyrrole is a complex organic chemical compound characterized by a pyrrole ring structure, which is a five-membered aromatic ring containing one nitrogen atom. 5-nitro-2-(trichloroacetyl)-1-methylpyrrole features a nitro group (-NO2) at the 5-position, a trichloroacetyl group (CCl3CO-) at the 2-position, and a methyl group (-CH3) at the 1-position. The trichloroacetyl group is a derivative of acetyl chloride, where three of the hydrogen atoms are replaced by chlorine atoms, enhancing the molecule's reactivity and stability. 5-nitro-2-(trichloroacetyl)-1-methylpyrrole may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and functional groups. However, it is important to note that the specific uses and properties of 5-nitro-2-(trichloroacetyl)-1-methylpyrrole would require further investigation and characterization.

53391-42-7

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53391-42-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53391-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,9 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53391-42:
(7*5)+(6*3)+(5*3)+(4*9)+(3*1)+(2*4)+(1*2)=117
117 % 10 = 7
So 53391-42-7 is a valid CAS Registry Number.

53391-42-7Relevant articles and documents

Synthesis of distamycin a polyamides targeting G-quadruplex DNA

Moore, Michael J. B.,Cuenca, Francisco,Searcey, Mark,Neidle, Stephen

, p. 3479 - 3488 (2006)

A number of amide-linked oligopyrroles based on distamycin molecules have been synthesized by solid-state methods, and their interactions with a human intramolecular G-quadruplex have been measured by a melting procedure. Several of these molecules show an enhanced ratio of quadruplex vs. duplex DNA binding compared to distamycin itself, including one with a 2,5-disubstituted pyrrole group. Quadruplex affinity increases with the number of pyrrole groups, and it is suggested that this is consistent with a mixed groove/G-quartet stacking binding mode. The Royal Society of Chemistry 2006.

Efficient synthesis of oligo-N-methylpyrrolecarboxamides and related compounds

Nishiwaki, Eiji,Tanaka, Shigeaki,Lee, Hideaki,Shibuya, Masayuki

, p. 1945 - 1952 (2007/10/02)

1-Methyl-4-nitro-2-trichloroacetylpyrrole 5, a new precursor for the syntheses of oligo-N-methylpyrrolecarboxamide antibiotics and their analogues, was prepared with facility. The versatility of 5 was demonstrated by the syntheses of oligopeptides 16-19.

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