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N-phenylundecanamide is an organic compound with the chemical formula C17H25NO. It is a derivative of undecanamide, where an unbranched alkyl chain of 11 carbon atoms is attached to an amide group, and a phenyl ring is connected to the nitrogen atom. N-phenylundecanamide is characterized by its long hydrocarbon chain and aromatic ring, which contribute to its unique chemical properties. It is a white crystalline solid and is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and other organic compounds. N-phenylundecanamide is not a high-volume chemical and is typically produced on a smaller scale for specific industrial purposes.

6911-89-3

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6911-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6911-89-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6911-89:
(6*6)+(5*9)+(4*1)+(3*1)+(2*8)+(1*9)=113
113 % 10 = 3
So 6911-89-3 is a valid CAS Registry Number.

6911-89-3Relevant academic research and scientific papers

Binuclear Pd(I)-Pd(I) Catalysis Assisted by Iodide Ligands for Selective Hydroformylation of Alkenes and Alkynes

Zhang, Yang,Torker, Sebastian,Sigrist, Michel,Bregovi?, Nikola,Dydio, Pawe?

supporting information, p. 18251 - 18265 (2020/11/02)

Since its discovery in 1938, hydroformylation has been thoroughly investigated and broadly applied in industry (>107 metric ton yearly). However, the ability to precisely control its regioselectivity with well-established Rh- or Co-catalysts has thus far proven elusive, thereby limiting access to many synthetically valuable aldehydes. Pd-catalysts represent an appealing alternative, yet their use remains sparse due to undesired side-processes. Here, we report a highly selective and exceptionally active catalyst system that is driven by a novel activation strategy and features a unique Pd(I)-Pd(I) mechanism, involving an iodide-assisted binuclear step to release the product. This method enables β-selective hydroformylation of a large range of alkenes and alkynes, including sensitive starting materials. Its utility is demonstrated in the synthesis of antiobesity drug Rimonabant and anti-HIV agent PNU-32945. In a broader context, the new mechanistic understanding enables the development of other carbonylation reactions of high importance to chemical industry.

Lewis acidity quantification and catalytic activity of Ti, Zr and Al-supported mesoporous silica

Zakharova, Maria V.,Kleitz, Freddy,Fontaine, Frédéric-Georges

supporting information, p. 3864 - 3876 (2017/03/31)

Water-tolerant supported Lewis acids are actively sought after, in particular to address the challenging direct amidation reaction. To this aim, a versatile and easy synthesis of large pore silica materials with supported Ti-, Al-, Zr-Lewis acids, using acetyl acetonate as a metal-stabilizing agent, was accomplished. The formation of bulk metal oxides was not observed, even at high concentrations of metal species. The Lewis acidity was demonstrated using quantitative and qualitative titration techniques using a series of Hammett indicators, such as butter yellow, phenylazodiphenylphosphine and dicinnamalacetone. The optimal concentration of metals corresponding to the highest Lewis acidity of solids was found to be 4% for Al-SBA-15, 12-15% for Ti-SBA-15 and 7% for Zr-SBA-15 materials. The water-tolerance of the supported metal centers was explored by a pyridine adsorption-FTIR study before and after water addition. The metalated materials were used as water-tolerant heterogeneous catalysts for the amidation of electron-poor and bulky amines, such as substituted anilines and morpholine, obtaining 59-99% yield of the corresponding amides.

Selective palladium-catalyzed aminocarbonylation of olefins with aromatic amines and nitroarenes

Fang, Xianjie,Jackstell, Ralf,Beller, Matthias

supporting information, p. 14089 - 14093 (2014/01/06)

Various olefins can be smoothly transformed in the presence of a Pd-based catalyst system and (hetero)aromatic amines or nitroarenes to synthetically interesting amides in good yields and often with high regioselectivity (see scheme). Combining this atom-efficient procedure with established functionalizations of the resulting products allows the efficient preparation of quinolines. Copyright

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