138376-46-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 13 carbon (C) atoms, 18 hydrogen (H) atoms, and 2 oxygen (O) atoms.
Explanation
This is the widely recognized name for the compound, which is derived from its characteristic fruity and sweet aroma that resembles raspberries.
Explanation
The compound is used in the fragrance and flavor industry due to its pleasant and distinctive scent, which can be used to enhance the aroma of various products.
Explanation
Research has shown that 1-Buten-2-ol, 1-(4-methylphenyl)-, propanoate, (E)- may have potential health benefits, such as aiding in weight management and acting as an antioxidant, which can help protect cells from damage caused by free radicals.
Explanation
The compound is used in the production and manufacturing of cosmetics and personal care products due to its pleasant aroma and potential health benefits.
Explanation
This term describes the specific arrangement of atoms and functional groups within the molecule, which determines its chemical properties and reactivity.
Explanation
The (E)prefix indicates the stereochemistry of the molecule, specifically the relative positions of the substituents around the double bond. In this case, the (E)configuration means that the two largest groups are on opposite sides of the double bond.
Explanation
The compound is likely to be soluble in organic solvents, such as ethanol, acetone, and diethyl ether, due to its nonpolar nature and the presence of hydrocarbon chains in its structure.
Explanation
Raspberry Ketone Acetate is generally stable under normal conditions, such as room temperature and pressure, and does not readily decompose or react with other substances. However, it may be sensitive to heat, light, or extreme pH conditions, which could affect its stability.
Usage in Fragrance and Flavor Industry
Fruity and Sweet Aroma
Potential Health Benefits
Weight Management and Antioxidant Properties
Application in Cosmetics and Personal Care Products
Production and Manufacturing
Application in Food Industry
Manufacturing of Food Products
Chemical Structure
1-Buten-2-ol, 1-(4-methylphenyl)-, propanoate, (E)-
Stereochemistry
(E)-
Solubility
Soluble in Organic Solvents
Stability
Stable under Normal Conditions
Check Digit Verification of cas no
The CAS Registry Mumber 138376-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,7 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138376-46:
(8*1)+(7*3)+(6*8)+(5*3)+(4*7)+(3*6)+(2*4)+(1*6)=152
152 % 10 = 2
So 138376-46-2 is a valid CAS Registry Number.
138376-46-2Relevant academic research and scientific papers
Electroreductive Acylation of Benzyl Chlorides with Acid Anhydrides. Stereoselective Formation of (E)-Enol Esters from Benzyl Alkyl Ketones
Nishiguchi, Ikuzo,Oki, Tsuneo,Hirashima, Tsuneaki,Shiokawa, Jiro
, p. 2005 - 2008 (2007/10/02)
Electroreduction of benzyl chlorides in the presence of acid anhydrides brought about stereoselective formation of (E)-enol esters of the corresponding benzyl alkyl ketones, the initial acylated products, in good to moderate yields.
