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2-furylmethyl 4-chlorobenzoate is an organic compound with the chemical formula C12H10ClO3. It is a colorless to pale yellow liquid with a fruity, floral, and green odor. 2-furylmethyl 4-chlorobenzoate is primarily used as a fragrance ingredient in various personal care products, such as perfumes, soaps, and lotions. It is also known for its potential use as a flavoring agent in food and beverages. The compound is synthesized through the esterification reaction between 4-chlorobenzoic acid and 2-furylmethanol. Due to its chemical structure, 2-furylmethyl 4-chlorobenzoate exhibits unique properties, making it a valuable component in the fragrance and flavor industry.

4449-28-9

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4449-28-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4449-28-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4449-28:
(6*4)+(5*4)+(4*4)+(3*9)+(2*2)+(1*8)=99
99 % 10 = 9
So 4449-28-9 is a valid CAS Registry Number.

4449-28-9Downstream Products

4449-28-9Relevant academic research and scientific papers

HMF and furfural: Promising platform molecules in rhodium-catalyzed carbonylation reactions for the synthesis of furfuryl esters and tertiary amides

Qi, Xinxin,Zhou, Rong,Ai, Han-Jun,Wu, Xiao-Feng

, p. 215 - 221 (2019/11/25)

A biomass involved rhodium-catalyzed carbonylative synthesis of furfuryl esters and tertiary amides has been developed. 5-Hydroxymethylfurfural (HMF) was used as both substrate and CO surrogate for the first time in a carbonylation reaction, and both alkyl and aryl iodides were tolerated well to afford the desired furfuryl esters in moderate to good yields. In addition, furfural was also utilized as a CO source for the synthesis of tertiary amides. A variety of tertiary amides were obtained in moderate to excellent yields with good functional groups compatibility. Notably, tertiary amines were used as the amine source through a C[sbnd]N bond cleavage pathway in the absence of additional oxidant.

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