93904-38-2 Usage
Description
(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)methyl cinnamate is a chemical compound with the molecular formula C17H20O2, characterized by its pleasant, sweet, and floral aroma. It is known for its potential antioxidant and anti-inflammatory properties, making it a versatile ingredient across various industries.
Uses
Used in Perfumery and Fragrance Industry:
(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)methyl cinnamate is used as a fragrance ingredient for its pleasant, sweet, and floral aroma, enhancing the scent profiles of perfumes and fragrances.
Used in Skincare Products:
In the skincare industry, (6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)methyl cinnamate is used as an active ingredient for its potential antioxidant and anti-inflammatory properties, contributing to the health and appearance of the skin.
Used in the Food Industry:
(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)methyl cinnamate is used as a flavoring agent, particularly in the production of fruit-flavored beverages and confectionery items, due to its sweet and floral taste.
Check Digit Verification of cas no
The CAS Registry Mumber 93904-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,0 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 93904-38:
(7*9)+(6*3)+(5*9)+(4*0)+(3*4)+(2*3)+(1*8)=152
152 % 10 = 2
So 93904-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H22O2/c1-19(2)16-10-9-15(17(19)12-16)13-21-18(20)11-8-14-6-4-3-5-7-14/h3-9,11,16-17H,10,12-13H2,1-2H3/b11-8+
93904-38-2Relevant articles and documents
Stevisalicinone, a New Diterpene Type, and Other Constituents from Stevia Species
Bohlmann, Ferdinand,Zdero, Christa
, p. 1764 - 1783 (2007/10/02)
From three Mexican Stevia species in addition to known compounds 25 new ones were isolated: myrthenyl cinnamate (1), the benzofurane derivatives 2, 3, and 5, a geranylnerol derivative (7), three sesquiterpene lactones (8-10), three labdane derivatives (11, 12, and 15), a cis-clerodane derivative (17), and a diterpene with a new carbon skeleton, named stevisalicinone (18) and biogenetically related to 17, as well as 12 longipinene derivatives (19-21, 25, 26, 28, 31, 33-35, 39, and 41).The stereochemistry of all derivatives is established by thorough NOE difference spectroscopy.
