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25035-85-2

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25035-85-2 Usage

Uses

Poly(tetrahydrofurfuryl methacrylate) may find potential uses in medical implants.

General Description

Poly(tetrahydrofurfuryl methacrylate) is biocompatible in nature. The structure of the polymer remains rigid even after absorbing water up to 75%. Large diffusion of water results in lowering of glass transition temperature.

Check Digit Verification of cas no

The CAS Registry Mumber 25035-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,3 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25035-85:
(7*2)+(6*5)+(5*0)+(4*3)+(3*5)+(2*8)+(1*5)=92
92 % 10 = 2
So 25035-85-2 is a valid CAS Registry Number.

25035-85-2Downstream Products

25035-85-2Relevant articles and documents

Dehydrogenative Silylation of Alkenes for the Synthesis of Substituted Allylsilanes by Photoredox, Hydrogen-Atom Transfer, and Cobalt Catalysis

Yu, Wan-Lei,Luo, Yong-Chun,Yan, Lei,Liu, Dan,Wang, Zhu-Yin,Xu, Peng-Fei

supporting information, p. 10941 - 10945 (2019/07/17)

A synergistic catalytic method combining photoredox catalysis, hydrogen-atom transfer, and proton-reduction catalysis for the dehydrogenative silylation of alkenes was developed. With this approach, a highly concise route to substituted allylsilanes has been achieved under very mild reaction conditions without using oxidants. This transformation features good to excellent yields, operational simplicity, and high atom economy. Based on control experiments, a possible reaction mechanism is proposed.

Producing unsaturated esters by a lanthanide metal alkoxide catalyzed transesterification process

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Example 5, (2008/06/13)

There is disclosed a process for producing an unsaturated ester of the formula (3): wherein R1, R2 and R3 independently represent hydrogen, halogen, alkyl, alkenyl and the like and R5 represents alkyl which may be substituted and the like, which process is characterized by subjecting an unsaturated ester of the formula (1): wherein R1, R2 and R3 have the same meaning as previously defined and R4 represents alkyl or phenyl and the like, to a transesterification reaction with a hydroxy compound of the formula (2):R5OH??(2)wherein R5 has the same meaning as previously defined, in the presence of a lanthanoide metal alkoxide.

Disinfectant polymeric coatings for hard surfaces

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, (2008/06/13)

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