1206615-69-1 Usage
Description
(2E)-3-(4-Hydroxy-3-methoxyphenyl)-2-propenoic acid (2E)-3,7-dimethyl-2,6-octadien-1-yl ester, also known as ferulic acid ethyl ester, is a natural plant compound that consists of a phenolic group and a propenoic acid ester. It is found in various foods such as grains, fruits, and vegetables and is known for its antioxidant properties.
Uses
Used in Health and Nutrition Industry:
(2E)-3-(4-Hydroxy-3-methoxyphenyl)-2-propenoic acid (2E)-3,7-dimethyl-2,6-octadien-1-yl ester is used as a dietary supplement for its potential health benefits, including its anti-inflammatory and anti-cancer properties. It helps to reduce inflammation and oxidative stress, and may also have a protective effect against certain types of cancer.
Used in Cosmetic and Skincare Industry:
(2E)-3-(4-Hydroxy-3-methoxyphenyl)-2-propenoic acid (2E)-3,7-dimethyl-2,6-octadien-1-yl ester is used as an ingredient in cosmetic and skincare products for its ability to protect the skin from UV damage. It has antioxidant and anti-inflammatory properties that can help to reduce the signs of aging and improve skin health.
Check Digit Verification of cas no
The CAS Registry Mumber 1206615-69-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,6,1 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1206615-69:
(9*1)+(8*2)+(7*0)+(6*6)+(5*6)+(4*1)+(3*5)+(2*6)+(1*9)=131
131 % 10 = 1
So 1206615-69-1 is a valid CAS Registry Number.
1206615-69-1Relevant articles and documents
Gd(OTf)3-catalyzed synthesis of geranyl esters for the intramolecular radical cyclization of their epoxides mediated by titanocene(III)
Garca Santos, William H.,Puerto Galvis, Carlos E.,Kouznetsov, Vladimir V.
, p. 1358 - 1366 (2015/02/05)
A selective and mild method for the esterification of a variety of carboxylic acids with geraniol is developed. We demonstrated that the use of triphenylphosphine, I2, 2-methylimidazole or imidazole and a catalytic amount of Gd(OTf)3 resulted to be more active than the previous protocols, providing a 16-membered library of geranyl esters in higher yields and in shorter reaction times. The use of essential oil of palmarosa (Cymbopogon martinii), enriched with geraniol, as a raw material for the synthesis of the target compounds complemented and proved how sustainable and eco-friendly this protocol is. Finally, the selective 6,7-epoxidation of the obtained geranyl esters led us to study their regio-controlled radical cyclization mediated by titanocene(iii) for the synthesis of novel (8-hydroxy-9,9-dimethyl-5-methylene cyclohexyl)methyl esters in moderate yields and with excellent stereoselectivities.
