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1-(4-butylphenyl)-2-hydroxyethan-1-one, also known as Heliotropin, is a chemical compound that belongs to the class of aromatic ketones. It is characterized by its sweet, powdery, and floral scent, which is reminiscent of vanilla, almond, and cherry.

1480233-72-4

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1480233-72-4 Usage

Uses

Used in Fragrance Industry:
1-(4-butylphenyl)-2-hydroxyethan-1-one is used as a fragrance ingredient for its sweet, powdery, and floral scent, which is reminiscent of vanilla, almond, and cherry. It is commonly added to perfumes, soaps, and cosmetic products to enhance their aroma.
Used in Flavor Industry:
In the flavor industry, 1-(4-butylphenyl)-2-hydroxyethan-1-one is used as a flavoring agent in various food products such as ice cream, baked goods, and beverages. Its unique scent and taste profile contribute to the overall flavor profile of these products, making them more appealing to consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 1480233-72-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,8,0,2,3 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1480233-72:
(9*1)+(8*4)+(7*8)+(6*0)+(5*2)+(4*3)+(3*3)+(2*7)+(1*2)=144
144 % 10 = 4
So 1480233-72-4 is a valid CAS Registry Number.

1480233-72-4Upstream product

1480233-72-4Downstream Products

1480233-72-4Relevant academic research and scientific papers

Aerobic Direct Dioxygenation of Terminal/Internal Alkynes to α-Hydroxyketones by an Fe Porphyrin Catalyst

Kimura, Kento,Kurahashi, Takuya,Matsubara, Seijiro

, p. 3615 - 3618 (2021)

We herein report a new synthetic method for the preparation of α-hydroxyketones by the dioxygenation of alkynes. The reaction proceeds at room temperature under the action of Fe porphyrin and pinacolborane under air as a green oxidant to produce α-hydroxyketones. The mild reaction conditions allow chemoselective oxidation with functional group tolerance. Terminal alkynes in addition to internal alkynes are applicable, affording unsymmetrical α-hydroxyketones that are difficult to obtain by any reported dioxygenation of unsaturated C?C bonds.

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