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Poly(tetrahydrofurfuryl methacrylate), also known as PTM, is a biocompatible polymer with a rigid structure that can absorb up to 75% water without losing its integrity. Its unique properties, such as maintaining rigidity and lowering the glass transition temperature upon water absorption, make it a promising material for various applications.

25035-85-2

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25035-85-2 Usage

Uses

Used in Medical Implants:
Poly(tetrahydrofurfuryl methacrylate) is used as a material for medical implants due to its biocompatibility and ability to maintain structural integrity even when absorbing large amounts of water. This makes it suitable for long-term implantation in the human body without causing adverse reactions or compromising its performance.

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 academic research and scientific papers

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.

PROCESS FOR PREPARING 4-HYDROXYBUTYL ACRYLATE

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Paragraph 0635; 0636; 0637; 0638; 0639, (2015/04/22)

A process for preparing 4-hydroxybutyl acrylate by transesterifying an alkyl acrylate with 1,4-butanediol in the presence of a dialkyltin oxide such that each of the alkyl groups has 4 to 8 carbon atoms, characterized in that the amount of the dialkyltin oxide is adjusted to 0.00001 to 0.01 moles per one mole of the alkyl acrylate.

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)

Liquid disinfectant compositions are disclosed which can be used to surface-coat substrates with polymeric films which are adherent, water-resistant and which can impart prolonged germicidal properties to the treated surfaces.

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