6561-39-3 Usage
Description
Hexyl nonan-1-oate is a liquid organic compound with a fresh vegetable and fruity aroma. It has medium strength odor and is classified as a floral type fragrance ingredient.
Uses
Used in Flavor and Fragrance Industry:
Hexyl nonan-1-oate is used as a flavor and fragrance ingredient for its fresh vegetable and fruity aroma. Its medium strength odor and floral type make it suitable for enhancing the scent of various products in the flavor and fragrance industry.
Used in Perfumery:
In the perfumery industry, hexyl nonan-1-oate is used as a fixative agent to help stabilize and prolong the scent of perfumes. Its floral type aroma adds a pleasant and long-lasting fragrance to perfume compositions.
Used in Cosmetics:
Hexyl nonan-1-oate is used as a fragrance ingredient in the cosmetics industry. Its fresh and fruity aroma enhances the sensory experience of cosmetic products, making them more appealing to consumers.
Used in the Food Industry:
In the food industry, hexyl nonan-1-oate is used as an additive to provide a pleasant and fresh aroma to various food products. Its medium strength odor and floral type make it suitable for enhancing the flavor and aroma of a wide range of food items.
Check Digit Verification of cas no
The CAS Registry Mumber 6561-39-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,6 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6561-39:
(6*6)+(5*5)+(4*6)+(3*1)+(2*3)+(1*9)=103
103 % 10 = 3
So 6561-39-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H30O2/c1-3-5-7-9-10-11-13-15(16)17-14-12-8-6-4-2/h3-14H2,1-2H3
6561-39-3Relevant articles and documents
Fluoride-Catalyzed Esterification of Amides
Wu, Hongxiang,Guo, Weijie,Daniel, Stelck,Li, Yue,Liu, Chao,Zeng, Zhuo
, p. 3444 - 3447 (2018/02/21)
In recent years, it has been demonstrated that amide carbon–nitrogen bonds can be activated and selectively cleaved using transition metal catalysts. However, these methodologies have been restricted to specific amides; a one-to-one relationship exists between the catalytic system and the amides and also uses large amounts of transition-metal catalysts and ligands. Hence, we now report a general strategy for esterification of common amides using fluoride as a catalyst. This method shows high functional group tolerance, and notably it requires only a slight excess of the alcohol nucleophile, which is a rare case in transition-metal-free amide transformations. Moreover, this approach may provide a new understanding for further studies on esterification of amides and is expected to stimulate the development of alternative methods for direct functionalization of amides.
