7541-49-3 Usage
Description
3,7,11,15-TETRAMETHYL-2-HEXADECEN-1-OL is a naturally occurring organic compound that is widely found in various plant species. It is characterized by its unique molecular structure, featuring a long hydrocarbon chain with four methyl groups at the 3rd, 7th, 11th, and 15th carbon positions. 3,7,11,15-TETRAMETHYL-2-HEXADECEN-1-OL is known for its distinct aroma and is commonly used in the fragrance industry.
Uses
Used in Fragrance Industry:
3,7,11,15-TETRAMETHYL-2-HEXADECEN-1-OL is used as a fragrance ingredient for its unique and pleasant scent. It is commonly incorporated into perfumes, colognes, and other scented products to provide a natural and appealing aroma.
Used in Flavor Industry:
In addition to its use in fragrances, 3,7,11,15-TETRAMETHYL-2-HEXADECEN-1-OL is also utilized as a flavoring agent in the food and beverage industry. Its distinct taste profile makes it suitable for enhancing the flavor of various products, such as beverages, confectionery, and savory foods.
Used in Cosmetics and Personal Care Products:
3,7,11,15-TETRAMETHYL-2-HEXADECEN-1-OL is employed in the formulation of cosmetics and personal care products, such as lotions, creams, and shampoos. Its pleasant scent and emollient properties contribute to the overall sensory experience and skin conditioning effects of these products.
Used in α-Tocopherol Analogs Preparation:
3,7,11,15-TETRAMETHYL-2-HEXADECEN-1-OL is used as a reagent in the preparation of α-tocopherol analogs, which are mitochondrial antioxidants. These analogs have potential applications in various industries, including pharmaceuticals and nutraceuticals, due to their antioxidant properties and potential health benefits.
Biochem/physiol Actions
Phytol exhibits potential anti-Schistosomal properties. It induces sedative and anxiolytic-like effects in mice.
Check Digit Verification of cas no
The CAS Registry Mumber 7541-49-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,4 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7541-49:
(6*7)+(5*5)+(4*4)+(3*1)+(2*4)+(1*9)=103
103 % 10 = 3
So 7541-49-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H40O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h15,17-19,21H,6-14,16H2,1-5H3
7541-49-3Relevant articles and documents
Preparation method of phytol and intermediates thereof
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Paragraph 0064-0099, (2021/03/18)
The invention discloses a preparation method of phytol and intermediates thereof, which comprises the following steps: (1) carrying out esterification rearrangement reaction on isophytol and anhydrideunder the action of perchlorate to obtain phytol ester; and (2) carrying out transesterification on the phytol ester to obtain the phytol. According to the preparation method disclosed by the invention, the total molar yield of the phytol can be up to 88.1%, the generation of potassium acetate or sodium acetate waste solids caused by a potassium hydroxide or sodium hydroxide hydrolysis process isavoided by adopting an ester exchange process, three wastes are effectively controlled, and the method is green and environment-friendly.
Synthesis method and method for synthesizing plant alcohol, isoplant alcohol and geranyl geraniol by using intermediate farnesylacetone (by machine translation)
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, (2020/07/21)
The invention relates to a synthesis method of intermediate farnesyl acetone and a method for synthesizing vitamin E, vitamin K1, vitamin K2 side chain isovegetable alcohol, plant alcohol and geranyl geraniol by using farnesyl acetone, and concretely relates to hydrogenation of 5 - farnesyl -2 - acetone and farnesyl acetone through three Grignard reaction to obtain plant ketone. The farnesyl acetone reacts with the vinyl chloride Grignard reagent to obtain geranyl linalool, the aromatic leaf-based geraniol is rearranged under acid catalysis, or farnesyl acetone is directly reacted with the hydroxyl-protected 2 - chloroethanol Grignard reagent to obtain geraniol. The plant alcohol is reacted with the vinyl chloride Grignard reagent to obtain the plant alcohol, and the plant alcohol is directly reacted with the hydroxyl-protected 2 - chloroethanol Grignard reagent to obtain the plant alcohol. The method has the advantages of cheap and easily available starting materials, short synthetic process steps, low product cost and the like. (by machine translation)