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(E)-(4-nitrostyryl)(phenyl)sulfane is an organic chemical compound characterized by a sulfur atom that is bonded to both a 4-nitrostyryl group and a phenyl group. The 4-nitrostyryl group features a nitro group attached to the 4-position of a styryl (phenylethenyl) moiety, while the phenyl group is a simple benzene ring. (E)-(4-nitrostyryl)(phenyl)sulfane is notable for its unique structure, which combines the properties of both aromatic and vinyl groups, and the presence of a sulfur atom that can participate in various chemical reactions. It is a yellow crystalline solid and is used in the synthesis of other organic compounds, particularly those involving sulfur-containing moieties. The compound's chemical formula is C14H11NO2S, and it has a molecular weight of 257.31 g/mol.

7214-55-3

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7214-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7214-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,1 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7214-55:
(6*7)+(5*2)+(4*1)+(3*4)+(2*5)+(1*5)=83
83 % 10 = 3
So 7214-55-3 is a valid CAS Registry Number.

7214-55-3Relevant academic research and scientific papers

Stereoselective heck reactions with vinyl sulfoxides, sulfides and sulfones

Bachmann, Daniel G.,Wittwer, Christopher C.,Gillingham, Dennis G.

, p. 3703 - 3707 (2013)

We report the Heck cross-coupling of notoriously unreactive, but synthetically valuable olefins: vinyl sulfoxides, vinyl sulfones, and vinyl sulfides. Key findings include the importance of the sterically hindered (tri-tert-butyl)phosphine ligand and the unique effectiveness of triethylamine as the base. The method is general, E-selective, and can be used to synthesize disubstituted or trisubstituted olefins through simple adjustments of stoichiometry. Copyright

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