Methyl cinnamate (CAS NO. 103-26-4), also known as Cinnamic acid methyl ester or Methyl trans-cinnamate, is the methyl ester of cinnamic acid. Methyl cinnamate is found naturally in a variety of plants, including in fruits, like strawberry, and some culinary spices, such as Sichuan pepper and some v
NAME: METHYL CINNAMATE SYNONYMS: CINNAMIC ACID METHYL ESTER; TRANS-CINNAMIC ACID METHYL ESTER; METHYL TRANS-CINNAMATE; METHYL 3-PHENYL-2-PROPENOATE; CINNAMIC ACID, METHYL ESTER, (E)- ODOR: SWEET, BALSAMIC WITH FRUITY ODOR, REMINISCENT OF CINNAMON AND STRAWBERRY
What is Methyl Cinnamate?Methyl cinnamate (CAS NO. 103-26-4) is the methyl ester of cinnamic acid and is a white or transparent solid with a strong, aromatic odor, a melting point of 33.5-36 ºC, a boiling point of 260-262 ºC. What else is Methyl Cinnamate called?
Methyl cinnamate is the methyl ester of cinnamic acid and is a white or transparent solid with a strong, aromatic odor. It is found naturally in a variety of plants, including in fruits, like strawberry, and some culinary spices, such as Sichuan pepper and some varieties of basil. Methyl cinnamate
Methyl cinnamate (CAS NO. 103-26-4) belongs to the class of organic compounds known as cinnamic acid esters. These are compound containing an ester derivative of cinnamic acid. Other names of methyl cinnamate: methyl trans-cinnamate, methyl e-cinnamate, cinnamic acid methyl ester, methyl cinnamylate
Whether it is stain or dark skin, it is related to melanin. The melanin bodies in melanocytes contain melanin and are therefore black. Analysis of the superficial stratum corneum of the yellow exposed area and the non-exposed area revealed that the skin surface of the exposed area contained mor
Methyl cinnamate suppliers in the study found that methyl cinnamate has a significant inhibitory effect on tyrosinase, can inhibit the activity of tyrosinase monophenols and diphenols enzyme activity. The inhibitory effect of monophenolase on tyrosinase was mainly manifested in the significant
The electroreduction reaction of methyl cinnamate on a boron-doped diamond (BDD) electrode was investigated. The hydrodimer, dimethyl 3,4-diphenylhexanedioate (racemate/meso = 74:26), was obtained in 85% yield as the major product, along with small amounts of cyclic methyl 5-oxo-2,3-diphenylcyclopentane-1-carboxylate