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Cis-4-t-butyl-2-phenyl-1,3-dioxolane is a cyclic 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 ring and a t-butyl group (C(CH3)3) attached to the fourth carbon. The "cis" configuration indicates that both substituents are on the same side of the ring. cis-4-t-butyl-2-phenyl-1,3-dioxolane is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals and fragrances.

4141-37-1

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4141-37-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4141-37-1 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 4141-37:
(6*4)+(5*1)+(4*4)+(3*1)+(2*3)+(1*7)=61
61 % 10 = 1
So 4141-37-1 is a valid CAS Registry Number.

4141-37-1Relevant academic research and scientific papers

Direct conversion of acetals to esters with high regioselectivity via O,P-acetals

Maegawa, Tomohiro,Otake, Kazuki,Goto, Akihiro,Fujioka, Hiromichi

supporting information; experimental part, p. 5648 - 5651 (2011/09/15)

A new direct conversion of O,O-acetals to esters via O,P-acetal intermediates was developed. The regioselective cleavage of unsymmetrical cyclic acetals occurred to give the more crowded esters as single isomers.

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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