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The chemical compound "C21H29N7O14P2" is a complex organic molecule that contains 21 carbon atoms, 29 hydrogen atoms, 7 nitrogen atoms, 14 oxygen atoms, and 2 phosphorus atoms. C21H29N7O14P2 is likely to be a nucleotide or a derivative of nucleotides, given the presence of a phosphate group (P2) and a ribose or deoxyribose sugar backbone, which are characteristic of nucleic acids. The nitrogen atoms suggest the presence of amino groups, which are common in the bases of nucleotides. The compound's structure and function would be crucial in biological systems, potentially playing a role in energy transfer, as part of coenzymes, or in the structure of DNA and RNA. The specific identity and role of C21H29N7O14P2 would depend on the arrangement of these atoms and the functional groups they form.

7013-03-8

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7013-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7013-03-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,1 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7013-03:
(6*7)+(5*0)+(4*1)+(3*3)+(2*0)+(1*3)=58
58 % 10 = 8
So 7013-03-8 is a valid CAS Registry Number.

7013-03-8Downstream Products

7013-03-8Relevant academic research and scientific papers

Determination of Formate in Natural Waters by a Coupled Enzymatic/High-Performance Liquid Chromatographic Technique

Kieber, David J.,Vaughan, Graham M.,Mopper, Kenneth

, p. 1654 - 1659 (1988)

An enzymatic method was developed to quantify formic acid in natural water samples at submicromolar concentrations.The method is based on the oxidation of formate by formate dehydrogenase with corresponding reduction of β-nicotinamide adenine dinucleotide (β-NAD+) to reduced β-NAD+ (β-NADH); β-NADH is quantified by reversed-phase high-performance liquid chromatograhy with fluorometric detection.An important feature of this method is that the enzymatic reaction occurs directly in aqueous media, even seawater, and does not require sample pretreatment other than sample filtration.The reaction proceeds at room temperature at a slightly alkaline pH (7.5-8.5) and is specific for formate with a detection limit of 0.5 μM (S/N = 4) for a 200-μL injection.The precision of the method was 4.6percent relative standard deviation (n = 6) for a 0.6 μM standard addition of formate to Sargasso seawater.Average recoveries of 2 μM additions of formate to seawater, porewater, or rain were 103, 103, and 87percent, respectively.Intercalibration with a Dionex ion chromatographic system showed an excellent agreement of 98percent.Concentrations of formate present in natural samples ranged from 0.2 to 0.8 μM for Biscayne Bay seawater, 0.4 to 10.0 μM for Miami rain, and 0.9 to 8.4 μM for Biscayne Bay sediment porewater.

TENTATIVES DE REGENERATION DU COENZYME NADH PAR REDUCTION ELECTROCHIMIQUE ET HYDROGENATION CATALYTIQUE

Bergel, Alain,Durliat, Helene,Comtat, Maurice

, p. 593 - 600 (2007/10/02)

Among the various attempts for the electrochemical reduction of NAD(1+) on a platinum electrode only those realized with an electrode submitted to repetitive potentiodynamic perturbations lead to NADH with very low rates.Hydrogenation by molecular hydrogen catalysed by platinum allows the transformation of about 50percent of NAD(1+) in β-NADH enzymatically active.The reaction is faster with platinized platinum.In both cases β-NADH evolves with time to give three non identified products.

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