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(1-13C)<(Ethoxycarbonyl)methylene>triphenylphosphorane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116757-53-0

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116757-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116757-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,7,5 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 116757-53:
(8*1)+(7*1)+(6*6)+(5*7)+(4*5)+(3*7)+(2*5)+(1*3)=140
140 % 10 = 0
So 116757-53-0 is a valid CAS Registry Number.

116757-53-0Relevant academic research and scientific papers

On the early steps of cineol biosynthesis in Eucalyptus globulus

Rieder, Christoph,Jaun, Bernhard,Arigoni, Duilio

, p. 2504 - 2513 (2007/10/03)

Samples of [4-2H1]-1-deoxyxylutose (17a) and [2-13C, 4-2H1]-1-deoxyxylulose (17b), have been prepared by modification of known procedures and fed in aqueous solution to twiglets of Eucalyptus globulus

Chemo-enzymatic synthesis of specifically stable-isotope labelled L-glutamic acid and 2-oxoglutaric acid

Cappon, J. J.,Baart, J.,Walle, G. A. M. van der,Raap, J.,Lugtenburg, J.

, p. 158 - 166 (2007/10/02)

(3-13C)-(4-13C)-,(5-13C)- and (3,4-13C2)-2-oxoglutaric acid were prepared starting from the simple 13C-enriched compounds: ethyl bromoacetate and paraformaldehyde, via a single reaction scheme on the gram scale in high yield.This reaction scheme allows specific 13C enrichment of every carbon position and any combination of positions. (3-13C)-,(4-13C)-, (5-13C), (3,4-13C2) and (15N)-L-glutamic acid were prepared by converting the corresponding 2-oxoglutaric acids via an enantioselective enzymatic conversion.The labelled L-glutamic acids and 2-oxoglutaric acids were characterized by 1H NMR, 13C NMR and mass spectrometry.

Synthesis of Precursors Suitable for Pyrolytic Fragmentation to Pentatetraenone

Brown, Roger F. C.,Coulston, Karen J.,Eastwood, Frank W.,Hill, Martin P.

, p. 215 - 224 (2007/10/02)

Reaction of 2-phenylselenopropanoyl chloride with methyl (triphenylphosphoranylidene)ethanoate yielded methyl 4-phenylselenopenta-2,3-dienoate (3).Distillation of the ester (3) gave dimethyl (E,E)-3',4'-dimethylcyclobut-3'-ene-1',2'-diylidenebisethanoate

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