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keronopsamide A is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1215701-60-2

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1215701-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1215701-60-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,5,7,0 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1215701-60:
(9*1)+(8*2)+(7*1)+(6*5)+(5*7)+(4*0)+(3*1)+(2*6)+(1*0)=112
112 % 10 = 2
So 1215701-60-2 is a valid CAS Registry Number.

1215701-60-2Upstream product

1215701-60-2Downstream Products

1215701-60-2Relevant academic research and scientific papers

Keronopsamides, a new class of pigments from marine ciliates

Guella, Graziano,Frassanito, Rita,Mancini, Ines,Sandron, Tommaso,Modeo, Letizia,Verni, Franco,Dini, Fernando,Petroni, Giulio

, p. 427 - 434 (2010)

New pigments with an unprecedented skeleton, named keronopsamides A-C, were isolated from, the marine ciliate Pseudokeronopsis riccii. The structure of the most abundant: secondary metabolite, keronopsamide A, was established through extended Nuclear Magnetic Resonance (NMR) analysis and mass spectrometric (MS) data obtained by using electrospray (ESI) and. matrix assisted laser desorption (MALDI) ionizations. Structures of the minor analogues (keronopsamide B and C) were inferred from 1H NMR, chemical correlation, and LC-MS measurements. The analysis of NOE dipolar couplings and quantum chemical calculations, carried out by density functional theory (DFT) on the pre-ferred, rotamers of keronopsamide A, suggested a fully planar structure with, amide bond, in anti stereochemistry capable to break down the extended conjugation of the whole π electronic system. Although the presence of a 2-substituted 3,4dibromo-pyrrole moiety is reminiscent of previously isolated metabolites isolated from, a cell extract of Pseudakeronopsis rubra (keronopsins), keronopsamides show a new molecular skeleton formally derived from a peptide-like condensation of a 3-pyrrolepropenoic acid with an unsaturated bromotyramine.

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