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2,4,6-Trimethyl-2,5-heptadien-1-ol, also known as linalool, is a naturally occurring organic compound that belongs to the terpene family. It is a colorless liquid with a strong, sweet, floral scent, reminiscent of lavender and citrus. Linalool is widely found in various plants, such as lavender, coriander, and rosewood, and is commonly used in the fragrance and flavor industries. It is also known for its potential therapeutic properties, including anti-inflammatory, analgesic, and antimicrobial effects. The chemical structure of linalool consists of a heptadienol backbone with three methyl groups attached at the 2nd, 4th, and 6th carbon positions, making it a versatile and valuable compound in both natural and synthetic applications.

2352-55-8

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2352-55-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2352-55-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2352-55:
(6*2)+(5*3)+(4*5)+(3*2)+(2*5)+(1*5)=68
68 % 10 = 8
So 2352-55-8 is a valid CAS Registry Number.

2352-55-8Relevant academic research and scientific papers

Termite trail attractants: New synthesis of racemic (E)-α-, (Z)-α- and β-bisabolenes

Argenti,Bellina,Carpita,Dell'Amico,Rossi

, p. 3167 - 3188 (1994)

Racemic (E)-α-bisabolene (E)(1) was synthetized starting from 4-methyl-3-cyclohexenecarboxylic acid (3) by a reaction sequence involving the Pd(0)-catalyzed cross-coupling reaction between the (E)-2-methyl-1-alkenyltrimethylstannane 8 and 3-methyl-2-buten-1-yl acetate (9). Three different procedures, in which a common precursor was used as key intermediate, were tested for the synthesis of racemic (Z)-α-bisabolene (Z)(1). The best one, which involved the reaction between bromide 18 and lithium dialkenylcuprate 19, afforded a mixture of (Z)- and (E)-1 in a 93:7 molar ratio, respectively. Finally, racemic β-bisabolene (2) was synthetized by a simple reaction sequence involving the Zr-promoted methylenation of ketone 22 prepared from 3.

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