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2-phenyl-4-(propan-2-yl)-1,3-dioxolane is an organic compound characterized by a 1,3-dioxolane ring, which consists of two oxygen atoms and three carbon atoms. The molecule features a phenyl group (C6H5) attached to the second carbon of the dioxolane ring and a propan-2-yl group (C3H7) attached to the fourth carbon. This structure contributes to its unique chemical properties and potential applications in various fields, such as pharmaceuticals and chemical synthesis. The compound's molecular formula is C12H16O2, and it has a molecular weight of 192.25 g/mol.

4141-35-9

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4141-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4141-35-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,4 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4141-35:
(6*4)+(5*1)+(4*4)+(3*1)+(2*3)+(1*5)=59
59 % 10 = 9
So 4141-35-9 is a valid CAS Registry Number.

4141-35-9Downstream Products

4141-35-9Relevant academic research and scientific papers

Oxidation Under Reductive Conditions: From Benzylic Ethers to Acetals with Perfect Atom-Economy by Titanocene(III) Catalysis

Funk, Pierre,Richrath, Ruben B.,Bohle, Fabian,Grimme, Stefan,Gans?uer, Andreas

, p. 5482 - 5488 (2021/02/03)

Described here is a titanocene-catalyzed reaction for the synthesis of acetals and hemiaminals from benzylic ethers and benzylic amines, respectively, with pendant epoxides. The reaction proceeds by catalysis in single-electron steps. The oxidative addition comprises an epoxide opening. An H-atom transfer, to generate a benzylic radical, serves as a radical translocation step, and an organometallic oxygen rebound as a reductive elimination. The reaction mechanism was studied by high-level dispersion corrected hybrid functional DFT with implicit solvation. The low-energy conformational space was searched by the efficient CREST program. The stereoselectivity was deduced from the lowest lying benzylic radical structures and their conformations are controlled by hyperconjugative interactions and steric interactions between the titanocene catalyst and the aryl groups of the substrate. An interesting mechanistic aspect is that the oxidation of the benzylic center occurs under reducing conditions.

DETERMINATION OF ENANTIOMERIC PURITY OF GLYCOLS RCHOHCH2OH

Eliel, Ernest L,Ko, Kwang-Youn

, p. 3547 - 3550 (2007/10/02)

The enantiomeric purity of primary-secondary glycols, RCHOHCH2OH, is conveniently determined by conversion to a pair of epimeric 1,3-dioxolanes through condensation with benzaldehyde, followed by nmr spectroscopy in presence of a chiral shift reagent with observation of the benzylic protons.

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