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1-methyl-4-(octan-2-ylsulfonyl)benzene is an organic compound with the molecular formula C15H22O2S. It is a derivative of benzene, featuring a methyl group at the 1st position and an octan-2-ylsulfonyl group at the 4th position. The octan-2-ylsulfonyl group consists of an octane chain with a sulfonyl group attached to the 2nd carbon atom. This chemical is characterized by its aromatic structure and the presence of a sulfonyl functional group, which can participate in various chemical reactions. It is a colorless liquid with a distinct odor and is insoluble in water but soluble in organic solvents. Due to its unique structure, 1-methyl-4-(octan-2-ylsulfonyl)benzene has potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.

1573-04-2

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1573-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1573-04-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1573-04:
(6*1)+(5*5)+(4*7)+(3*3)+(2*0)+(1*4)=72
72 % 10 = 2
So 1573-04-2 is a valid CAS Registry Number.

1573-04-2Downstream Products

1573-04-2Relevant academic research and scientific papers

Nickel-Catalyzed Enantioconvergent Reductive Hydroalkylation of Olefins with α-Heteroatom Phosphorus or Sulfur Alkyl Electrophiles

Fu, Yao,He, Shi-Jiang,Li, Yan,Lu, Xi,Wang, Jia-Wang,Wang, Xiao-Xu,Xu, Zhe-Yuan

supporting information, (2020/01/22)

Substantial advances in enantioconvergent C(sp3)-C(sp3) bond formation reactions have been made in recent years through the use of transition-metal-catalyzed cross-coupling reactions of racemic secondary alkyl electrophiles with organometallic reagents. Herein, we report a general process for the asymmetric construction of alkyl-alkyl bonds adjacent to heteroatoms, namely, a nickel-catalyzed enantioconvergent reductive hydroalkylation of olefins with α-heteroatom phosphorus or sulfur alkyl electrophiles. Including the use of readily available olefins, this reaction has considerable advantages, such as mild reaction conditions, a broad substrate scope, and good functional group compatibility, making it a desirable alternative to traditional electrophile-nucleophile cross-coupling reactions.

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