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1,1-Dimethyl-2-(3-methyl-but-3-ene-1-sulfonyl)-ethyl-benzene is a complex organic compound with the molecular formula C16H22O2S. It is a derivative of benzene, featuring a sulfonyl group attached to a 3-methylbut-3-ene-1-yl moiety, which is in turn connected to a dimethylated ethyl group. [1,1-Dimethyl-2-(3-methyl-but-3-ene-1-sulfonyl)-ethyl]-benzene is characterized by its unique structure, which includes a benzene ring, a sulfonyl group, and an alkenyl chain. It is a synthetic chemical that may have applications in the fields of pharmaceuticals, agrochemicals, or as an intermediate in the synthesis of other organic compounds. Due to its specific functional groups and structural features, it can participate in various chemical reactions, such as nucleophilic substitutions, eliminations, and additions, making it a potentially valuable building block in organic synthesis.

87567-33-7

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87567-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87567-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,6 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87567-33:
(7*8)+(6*7)+(5*5)+(4*6)+(3*7)+(2*3)+(1*3)=177
177 % 10 = 7
So 87567-33-7 is a valid CAS Registry Number.

87567-33-7Downstream Products

87567-33-7Relevant academic research and scientific papers

Regio- and Stereoselective Hydrosulfonylation of Conjugated Dienes via a (?-Allyl)palladium Complex

Tamaru, Yoshinao,Yamada, Yoshimi,Kagotani, Masahiro,Ochiai, Hirofumi,Nakajo, Eiji,et al.

, p. 4669 - 4681 (2007/10/02)

The combination of a sulfonylpalladation of acyclic dienes 1 (with 2 equiv of NaSO2R and 1 equiv of PdCl2 in acetic acid or acetic acid-H2O at 50-80 deg C under air) and a protiodepalladation of the thus obtained palladium complexes 3 with dimethylglyoxime (in a protic solvent at room temperature) provides di- and trisubstituted (Z)-Δ3-sulfones 12 selectively, irrespective of the stereochemistry of the starting dienes.Similar treatment of 1-vinylcycloalkenes 5 (n (1,3) strain between Pd and the substituent on the allylic position.

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