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1-(1,3-Dimethyl-2-butenyl)-4-(trifluoromethyl)benzene, also known as a chemical compound with the molecular formula C12H13F3, is a colorless liquid characterized by a strong, sweet odor. It is recognized for its applications in various industries due to its distinct properties.

74764-29-7

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74764-29-7 Usage

Uses

Used in Fragrance Industry:
1-(1,3-Dimethyl-2-butenyl)-4-(trifluoromethyl)benzene is used as a fragrance ingredient for its strong, sweet odor, contributing to the creation of perfumes and personal care products. Its appealing scent enhances the sensory experience of these products, making them more attractive to consumers.
Used in Food Industry:
In the food industry, 1-(1,3-Dimethyl-2-butenyl)-4-(trifluoromethyl)benzene is utilized as a flavoring agent. Its unique taste and aroma add depth and complexity to various food products, enhancing their overall flavor profile and consumer appeal.
Used in Environmental Monitoring:
1-(1,3-Dimethyl-2-butenyl)-4-(trifluoromethyl)benzene has been identified as a potential environmental pollutant. As a result, it is used in environmental monitoring and assessment to detect and quantify its presence in aquatic ecosystems. This helps in understanding its potential impact on aquatic organisms and informs proper handling and disposal procedures to minimize its adverse effects on the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 74764-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,6 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74764-29:
(7*7)+(6*4)+(5*7)+(4*6)+(3*4)+(2*2)+(1*9)=157
157 % 10 = 7
So 74764-29-7 is a valid CAS Registry Number.

74764-29-7Downstream Products

74764-29-7Relevant academic research and scientific papers

Remote Arylative Substitution of Alkenes Possessing an Acetoxy Group via β-Acetoxy Elimination

Kakiuchi, Fumitoshi,Kochi, Takuya,Kumagai, Takaaki,Muto, Kazuma

, p. 24500 - 24504 (2021)

Palladium-catalyzed remote arylative substitution was achieved for the reaction of arylboronic acids with alkenes possessing a distant acetoxy group to provide arylation products having an alkene moiety at the remote position. The use of β-acetoxy elimination as a key step in the catalytic cycle allowed for regioselective formation of unstabilized alkenes after chain walking. This reaction was applicable to various arylboronic acids as well as alkene substrates.

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