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5-TERT-BUTYL-2-HYDROXY-3-HYDROXYMETHYLBENZALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39117-96-9

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39117-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39117-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,1 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39117-96:
(7*3)+(6*9)+(5*1)+(4*1)+(3*7)+(2*9)+(1*6)=129
129 % 10 = 9
So 39117-96-9 is a valid CAS Registry Number.

39117-96-9Relevant academic research and scientific papers

Lower rim 1,3-diderivative of calix[4]arene-appended salicylidene imine (H2L): Experimental and computational studies of the selective recognition of H2L toward Zn2+ and sensing phosphate and amino acid by [ZnL]

Joseph, Roymon,Chinta, Jugun Prakash,Rao, Chebrolu P.

experimental part, p. 3387 - 3395 (2010/08/03)

A new 1,3-diderivative of calix[4]arene appended with hydroxymethyl salicylyl imine has been synthesized and its ion recognition toward biologically relevant Mn+ ions studied. The receptor H2L showed selectivity toward Zn2+/sup

Studies on enzyme-cleavable dialkoxymethyl-cycloSaligenyl-2′, 3′-dideoxy-2′,3′-didehydrothymidine monophosphates

Gisch, Nicolas,Balzarini, Jan,Meier, Chris

experimental part, p. 6752 - 6760 (2009/11/30)

Recently we reported on conceptually new enzymatically activated cycloSal-pronucleotides. Now, we developed this concept further with new compounds of this type. The basic idea is fast intracellular cleavage of a functionalized group at the cycloSal residue that results in a rapid delivery of the nucleotide and thus an intracellular enrichment of the nucleotide. The introduction of a higher alkylated acylal group, the di-iso-butyryloxymethyl group, to the aromatic ring led to the expected higher stability of these prodrugs against enzymatic cleavage but also entailed surprisingly a decrease in hydrolysis stabilities and solubility problems. For some compounds, a separation of the two diastereomeric forms (RP or SP) was achieved. By X-ray structure analysis, the absolute configuration at the P-atom was assigned. For all separated diastereomers the (SP) form showed better antiviral activity than the (RP) form.

Synthesis and conformational aspects of 20- and 40-membered macrocyclic mono and dinuclear uranyl complexes incorporating salen and (R)-BINOL units

Amato, Maria E.,Ballistreri, Francesco P.,Pappalardo, Andrea,Sciotto, Domenico,Tomaselli, Gaetano A.,Toscano, Rosa Maria

, p. 9751 - 9757 (2008/02/13)

20- and 40-membered macrocyclic mono and dinuclear uranyl complexes 11-13 incorporating salen and (R)-BINOL units have been designed and synthesized starting from 4-tert-butylphenol in eight steps. NMR measurements (COSY, NOESY/EXSY) indicate that such co

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