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(3R,6R)-6-hydroxyhexahydrofuro[3,2-b]furan-3-yl acetate is a complex organic compound characterized by its unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, with the R configuration at both the 3 and 6 positions. (3R,6R)-6-hydroxyhexahydrofuro[3,2 b]furan-3-yl acetate features a hexahydrofuro[3,2-b]furan ring system, which is a type of furan derivative with six carbon atoms in a cyclic structure, including one oxygen atom. The 6-hydroxy group indicates the presence of a hydroxyl group attached to the sixth carbon, while the acetate group is attached to the third carbon, forming an ester linkage. This specific arrangement of functional groups and stereochemistry gives the compound distinct chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

73952-88-2

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73952-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73952-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,5 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73952-88:
(7*7)+(6*3)+(5*9)+(4*5)+(3*2)+(2*8)+(1*8)=162
162 % 10 = 2
So 73952-88-2 is a valid CAS Registry Number.

73952-88-2Relevant academic research and scientific papers

Isohexide hydroxy esters: Synthesis and application of a new class of biobased AB-type building blocks

Thiyagarajan, Shanmugam,Wu, Jing,Knoop, Rutger J. I.,Van Haveren, Jacco,Lutz, Martin,Van Es, Daan S.

, p. 47937 - 47950 (2014/12/10)

Here we present the synthesis of a new family of sugar derived 1,4:3,6-dianhydrohexitol based AB-type monomers, containing one methyl ester group and a secondary hydroxyl group in all four possible stereo isomers (RR, RS, SR, SS). Structural characterization of the monomers (5a-d) was established by 1D and 2D NMR analysis, which was further confirmed by single-crystal X-ray structure determination. The application of these monomers in step-growth polymerization afforded fully isohexide based stereo-regular polyesters. Homo polyesters based on the RR and RS monomers were obtained with reasonable molecular weights by melt polymerization (Mn 2400 and 2500 resp.). These materials showed unexpectedly low glass-transition temperatures of 20°C and 15°C respectively. In contrast, the monomers with SR and SS configuration yielded only low molecular weight oligomers. Surprisingly, copolymerization of the RR and SR monomers gave a polyester with higher molecular weight (Mn 4100) and a high Tg of 80°C. These preliminary results show that isohexide hydroxyesters are an intriguing new class of biobased building blocks with many potential applications.

Some Applications of Isopropenyl Acetate to O-, N- and C-Acetylation

Gizur, Tibor,Harsanyi, Kalman

, p. 2365 - 2371 (2007/10/02)

New procedure for the preparation of drugs and drug intermediates (isosorbide-5-nitrate, diltiazem) and intermediates of potential drugs using isopropenyl acetate are described.

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