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4-Vinyl-benzoic acid butyl ester is an organic compound with the chemical formula C13H16O2. It is a colorless to pale yellow liquid with a fruity, floral, and green odor. This ester is derived from 4-vinylbenzoic acid and butanol, and it is commonly used as a fragrance ingredient in various personal care products, such as perfumes, soaps, and lotions. It is also employed in the flavor industry to impart a fruity, green, and floral taste to food and beverages. The compound is known for its stability and is considered safe for use in these applications. However, it is important to note that, like any chemical, it should be handled with care and used in accordance with safety guidelines to avoid potential health or environmental risks.

2715-41-5

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2715-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2715-41-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,1 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2715-41:
(6*2)+(5*7)+(4*1)+(3*5)+(2*4)+(1*1)=75
75 % 10 = 5
So 2715-41-5 is a valid CAS Registry Number.

2715-41-5Downstream Products

2715-41-5Relevant academic research and scientific papers

PALLADIUM(0) AND RHODIUM(I) CATALYSIS OF THE CARBONYLATION OF UNACTIVATED BROMIDES

Hashem, Khaled E.,Woell, James B.,Alper, Howard

, p. 4879 - 4880 (1984)

Alkyl, vinyl, and aromatic bromides react with organoborates and carbon monoxide, in the presence of catalytic quantities of 1,5-hexadienerhodium(I) chloride dimer and tetrakis(triphenylphosphine)palladium(0), to give carboxylic esters in good yields.

An improved protocol for palladium-catalyzed alkoxycarbonylations of aryl chlorides with alkyl formates

Schareina, Thomas,Zapf, Alexander,Cotte, Alain,Gotta, Matthias,Beller, Matthias

experimental part, p. 1205 - 1209 (2010/07/04)

The palladium-catalyzed alkoxycarbonylation of aryl and heteroaryl halides using butyl formate has been investigated. In the presence of palladium (II) acetate/n-butylbis(1-adamantyl)phosphine (L1), and l,8-diazabicyclo[5.4.0]undec- 7-ene (DBU) as base fo

Palladium-Catalyzed Cross-Coupling Reaction of Organoindiums with Aryl Halides in Aqueous Media

Takami, Kazuaki,Yorimitsu, Hideki,Shinokubo, Hiroshi,Matsubara, Seijiro,Oshima, Koichiro

, p. 1997 - 1998 (2007/10/03)

(matrix presented) Diaryl-, divinyl-, and dialkylindium proved to be stable in aqueous media and to undergo a palladium-catalyzed cross-coupling reaction with aryl halides in aqueous THF. Treatment of 3-iodophenol with diphenylindium compound, generated from indium trichloride and two equimolar amounts of a phenyl Grignard reagent, in aqueous media under palladium catalysis provided the corresponding coupling product in excellent yield. Divinyl- and diethlindium can be used for the coupling reaction in the presence of water. A wide range of functional groups, including a hydroxy group and a formyl group, are compatible with this reaction.

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