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2-((E)-3-Phenyl-pent-2-enyl)-[1,3]dithiane-2-carbaldehyde is a complex organic compound characterized by a unique molecular structure. It features a dithiane ring, which is a sulfur-containing heterocyclic compound, and an aldehyde group, indicating the presence of a carbonyl group at the end of a carbon chain. The compound also includes a phenyl group, which is a benzene ring, and a pent-2-enyl chain, signifying a five-carbon chain with a double bond between the second and third carbon atoms. The "E" notation in the name suggests that the double bond has the E-configuration, which refers to the geometric arrangement of the substituents around the double bond. 2-((E)-3-Phenyl-pent-2-enyl)-[1,3]dithiane-2-carbaldehyde is likely to be found in the field of organic chemistry, potentially used in the synthesis of pharmaceuticals, fragrances, or other specialty chemicals due to its diverse functional groups and structural features.

97938-55-1

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97938-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97938-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,3 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97938-55:
(7*9)+(6*7)+(5*9)+(4*3)+(3*8)+(2*5)+(1*5)=201
201 % 10 = 1
So 97938-55-1 is a valid CAS Registry Number.

97938-55-1Downstream Products

97938-55-1Relevant academic research and scientific papers

The synthesis and characterization of 3,3-disubstituted pent-4-enals and their 2,2-(trimethylendithio)pent-4-enal precursors, including the X-ray crystal structure of (R)-3-ethyl-3-phenyl-2,2-(trimethylenedithio)pent-4-enal

Young, Charles G.,James, Brian R.,Rettig, Steven J.

, p. 1035 - 1040 (2007/10/02)

A variety of 3,3-disubstituted pent-4-enals (5a, R=Me, R'=Et; 5b, R=Me, R'=Ph; 5c, R=Et, R'=Ph) has been prepared by the Raney nickel desulfurization of the corresponding 3,3-disubstituted 2,2-(trimethylenedithio)pent-4-enal precursors 4a-4c.The precursor compounds were prepared by the alkylation of 2-formyl-1,3-dithiane with the appropriate 3,3-disubstituted allylic bromide.The new compounds have been characterized by elemental analysis, infrared and nmr spectroscopy, and mass spectrometry.The crystal and molecular structure of (R)-4c has also been determined by X-ray crystallography.At temperatures of ca. 130 deg C, compounds 4a-4c undergo intramolecular rearrangement to form the trisubstituted alkenes 6a-6c, which have also been characterized by the present study.

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