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2(5H)-Furanone, 5-hydroxy-5-(hydroxymethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95016-85-6

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95016-85-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95016-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,1 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95016-85:
(7*9)+(6*5)+(5*0)+(4*1)+(3*6)+(2*8)+(1*5)=136
136 % 10 = 6
So 95016-85-6 is a valid CAS Registry Number.

95016-85-6Upstream product

95016-85-6Downstream Products

95016-85-6Relevant academic research and scientific papers

Visible photostability of some ruthenium and platinum phthalocyanines in water and in the presence of organic substrates

Carchesio, Manuela,Tonucci, Lucia,D'Alessandro, Nicola,Morvillo, Antonino,Boccio, Piero Del,Bressan, Mario

, p. 499 - 508 (2010)

Water-soluble, metal-tetrasubstituted phthalocyanines (-SO3H, MPcS and -COOH, MPcC) of platinum and ruthenium were synthesized and their photostability to visible light irradiation was determined. For the ruthenium phthalocyanines, the characte

(2+4)-Cycloaddition with singlet oxygen. 17O-investigation of the reactivity of furfuryl alcohol endoperoxide

Braun, André M.,Dann, Hans,Gassmann, Ernst,Gerothanassis, Ioannis,Jakob, Laurent,Kateva, Jordanka,Martinez, Claudia G.,Oliveros, Esther

, p. 868 - 874 (2007/10/03)

In earlier work, the use of furfuryl alcohol as a specific singlet oxygen acceptor was proposed because of the high ratio between the rate constants of chemical reaction and physical quenching. In contrast to furfuryl aldehyde, a number of products are formed by this type II photooxidation of furfuryl alcohol. These products may be derived from the endoperoxide of furfuryl alcohol as a common intermediate. The present work focuses on the reactivity of this endoperoxide that was marked specifically by the use of 17O2 as a source for singlet oxygen. The analyses of the stable products, their yields and their labeling distribution reveal a strong solvent effect on the primary reaction pathways, and nucleophilic substitution reactions leading to hydroperoxide intermediates are dominant.

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