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Benzene, 1,3-bis(1,1-dimethylethyl)-5-methyl-2-(2-propenyloxy)-, also known as 1,3,5-trimethyl-2-(2-propenyloxy)benzene, is an organic compound with the molecular formula C13H20O. It is a colorless liquid with a density of 0.87 g/cm3 and a boiling point of 250°C. Benzene, 1,3-bis(1,1-dimethylethyl)-5-methyl-2-(2-propenyloxy)- is characterized by its benzene ring structure, with three methyl groups (CH3) attached at the 1, 3, and 5 positions, and a 2-propenyloxy (allyloxy) group at the 2 position. The 2-propenyloxy group consists of a propene (allyl) chain with an oxygen atom attached to the terminal carbon. This chemical is primarily used as a fragrance ingredient and a synthetic intermediate in the production of various chemicals, such as pharmaceuticals and agrochemicals. Due to its complex structure and specific functional groups, it exhibits unique chemical properties and reactivity, making it a valuable compound in the field of organic chemistry.

1516-98-9

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1516-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1516-98-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1516-98:
(6*1)+(5*5)+(4*1)+(3*6)+(2*9)+(1*8)=79
79 % 10 = 9
So 1516-98-9 is a valid CAS Registry Number.

1516-98-9Relevant academic research and scientific papers

Investigating the microwave-accelerated Claisen rearrangement of allyl aryl ethers: Scope of the catalysts, solvents, temperatures, and substrates

Hui, Zi,Jiang, Songwei,Qi, Xiang,Ye, Xiang-Yang,Xie, Tian

, (2020)

The microwave-accelerated Claisen rearrangement of allyl aryl ethers was investigated, in order to gain insight into the scope of the catalysts, solvents, temperatures, and substrates. Among the catalysts examined, phosphomolybdic acid (PMA) was found to greatly accelerate the reaction in NMP, at temperatures ranging from 220 to 300 °C. This method was found to be useful for preparing several intermediates previously reported in the literature using precious metal catalysts such as Au(I), Ag(I), and Pt(II). Additionally, substrates bearing bromo and nitro groups on the aryl portion required careful tailoring of the reaction conditions to avoid complex product profiles.

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