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Benzene, 1-ethenyl-4-(1-methylbutyl)-, also known as 1-vinyl-4-isopentylbenzene or more commonly as p-isopropenyltoluene, is an organic compound with the chemical formula C12H16. It is a colorless liquid with a strong aromatic odor and is derived from the reaction of benzene with isopentylene. Benzene, 1-ethenyl-4-(1-methylbutyl)- is primarily used as an intermediate in the production of various chemicals, such as antioxidants and resins, and plays a significant role in the synthesis of polymers and other industrial chemicals. Due to its reactive nature, it is essential to handle p-isopropenyltoluene with proper safety measures to avoid potential health and environmental risks.

7641-98-7

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7641-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7641-98-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,4 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7641-98:
(6*7)+(5*6)+(4*4)+(3*1)+(2*9)+(1*8)=117
117 % 10 = 7
So 7641-98-7 is a valid CAS Registry Number.

7641-98-7Downstream Products

7641-98-7Relevant academic research and scientific papers

FLASH VACUUM THERMOLYSIS OF DISPIROALKADIENES

Kraakmann, P. A.,Nibbering, E. T. J.,Wolf, W. H. de,Bickelhaupt, F.

, p. 5109 - 5124 (2007/10/02)

The Flash Vacuum Thermolysis (FVT) of dispirotetradeca -4,13-diene (7a). dispirotrideca-4,12-diene (7b) and dispirodeca-4,9-diene (7e) at 500-750 deg C is reported.The complicated reaction mixture from 7a and 7b (Scheme 3) included at lower temperatures vinylspiroalkadienes 9, ethylidenespiroalkadiene 10b, β-ethylcycloalkabenzenes 11, while at higher temperatures, p-n-alkyl-(5) and p-sec-alkylstyrenes 14 and p-divinylbenzene (15) dominated.Product formation is explained by invoking diradicals 8,6 and 12 as well as the cyclophanes 1 and 13 as intermediates.For 7e, the product mixture was less complicated and consisted of p-ethylstyrene (5e), 15 and, unexpectedly,p-isopropylstyrene (14e) which contains one carbon more than the starting material.The analysis and interpretation of product formation largely confirms previously suggested reaction pathways and furnishes further interesting details.However, new and unexpected features are also encountered, especially in the fragmentations of 1 and 13 which may stimulate future investigations on the thermal behaviour of these relatively simple hydrocarbons.

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