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4-Butoxy-3-penten-2-one is an organic compound with the molecular formula C9H16O2. It is a colorless liquid with a fruity, floral odor and is commonly used as a fragrance ingredient in various personal care products, such as perfumes, soaps, and lotions. This chemical is also known as 4-Butyloxy-3-penten-2-one or Butyl 3-pentenoate and is characterized by its molecular weight of 156.22 g/mol. It is insoluble in water but soluble in organic solvents. The compound is synthesized through the reaction of butanol with 3-penten-2-one, and it is used in the production of various flavorings and fragrances due to its pleasant aroma.

3431-87-6

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3431-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3431-87-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,3 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3431-87:
(6*3)+(5*4)+(4*3)+(3*1)+(2*8)+(1*7)=76
76 % 10 = 6
So 3431-87-6 is a valid CAS Registry Number.

3431-87-6Downstream Products

3431-87-6Relevant academic research and scientific papers

Alkylation Reactions of Ethyl Malonate, Ethyl Acetoacetate, and Acetylacetone by Gas-Liquid Phase-Transfer Catalysis (G.L.-P.T.C)

Tundo, Pietro,Venturello, Paolo,Angeletti, Enrico

, p. 2159 - 2162 (2007/10/02)

Malonyl, acetoacetyl, and acetylacetonyl alkylation reactions have been carried out in the gaseous state under gas-liquid phase-transfer catalysis (g.l-p.t.c) conditions using potassium carbonate or sodium hydrogencarbonate as the base.No alkali metal was used to generate the reactive anion.No solvents are used in the process, and the reaction mixture requires no stirring.The phase-transfer catalysts which promote the reaction: phosphonium salts, crown ethers, and poly(ethylene glycol) are also the medium in which the reaction occurs; they direct C- or O- alkylation, as a function of the methylene compound and the alkylating agent used.The malonic ester alkylation using poly(ethylene glycol) gives rise to improved selectivity for C-monoalkylation compared with the other catalysts.

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