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(2S)-2,3-dihydroxypropyl methacrylate is a chiral monomer with the chemical formula C7H12O4. It is a derivative of methacrylate, featuring two hydroxyl groups at the 2nd and 3rd carbon positions of the propyl chain, and an (S)-configuration at the chiral center. (2S)-2,3-dihydroxypropyl methacrylate is used in the synthesis of polymers with specific properties, such as improved hydrophilicity and biocompatibility, making it valuable in the fields of biomedical materials and drug delivery systems. Its unique structure allows for the creation of polymers that can interact with biological systems, potentially leading to advanced materials for medical applications.

96557-24-3

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96557-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96557-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,5 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96557-24:
(7*9)+(6*6)+(5*5)+(4*5)+(3*7)+(2*2)+(1*4)=173
173 % 10 = 3
So 96557-24-3 is a valid CAS Registry Number.

96557-24-3Downstream Products

96557-24-3Relevant academic research and scientific papers

Chiral polyamino alcohols and polyamino thiols for asymmetric heterogeneous catalysis

Herault, Damien,Saluzzo, Christine,Lemaire, Marc

, p. 1944 - 1951 (2006)

A series of macroporous copolymer beads were synthesized by THE free radical suspension copolymerization of (S)-glycidylmethacrylate (GMA), (S)-thiiranylmethylmethacrylate (TMA), or (R,R)-phenylglycidylmethacrylate (Ph-GMA) with ethyleneglycol dimethacryl

Enantiopure poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate): A new material for supported catalytic asymmetric hydrogen transfer reduction

Rolland, Alice,Herault, Damien,Touchard, Francois,Saluzzo, Christine,Duval, Raphael,Lemaire, Marc

, p. 811 - 815 (2007/10/03)

A novel copolymer containing chiral epoxy residues was prepared. Free radical initiated suspension copolymerization of (R)- or (S)-glycidyl methacrylate with ethylene glycol dimethacrylate afforded crosslinked copolymer 1 in high yield. Optically active polymers containing amino alcohol functionalities were then formed from 1 through epoxide ring opening with a number of achiral and homochiral amines. It was shown that ruthenium complexes based on these new polymeric amino alcohol ligands were effective catalysts for the asymmetric hydrogen transfer reduction of acetophenone.

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