169376-35-6 Usage
Description
ETHYL-2-PYRROLOYL-ACETATE is a chemical compound characterized by its molecular formula C8H11NO2. It is an ester that features a pyrrole ring structure, known for its sweet, fruity odor with floral and woody undertones. ETHYL-2-PYRROLOYL-ACETATE is widely recognized for its applications in various industries, particularly for its use as a flavoring and fragrance ingredient.
Uses
Used in Perfume Industry:
ETHYL-2-PYRROLOYL-ACETATE is used as a flavoring and fragrance ingredient for its sweet, fruity scent with floral and woody notes, enhancing the aroma profiles of perfumes and creating a pleasant olfactory experience.
Used in Food Industry:
In the food industry, ETHYL-2-PYRROLOYL-ACETATE is utilized as a component in artificial fruit flavors, adding a natural and appealing taste to various food products.
Used in Cosmetics Industry:
ETHYL-2-PYRROLOYL-ACETATE is employed in the formulation of scented products such as soaps and lotions, where it imparts a pleasant fragrance and contributes to the overall sensory appeal of these products.
Used in Pharmaceutical Manufacturing:
ETHYL-2-PYRROLOYL-ACETATE also serves as a solvent and is involved in the manufacturing process of pharmaceuticals, playing a role in the development of various medicinal compounds.
Used in Chemical Compounds Production:
ETHYL-2-PYRROLOYL-ACETATE is used in the production of other chemical compounds, highlighting its versatility and importance in the realm of chemical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 169376-35-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,3,7 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 169376-35:
(8*1)+(7*6)+(6*9)+(5*3)+(4*7)+(3*6)+(2*3)+(1*5)=176
176 % 10 = 6
So 169376-35-6 is a valid CAS Registry Number.
169376-35-6Relevant articles and documents
Bromide-Mediated C-H Bond Functionalization: Intermolecular Annulation of Phenylethanone Derivatives with Alkynes for the Synthesis of 1-Naphthols
Lu, Tao,Jiang, Ya-Ting,Ma, Feng-Ping,Tang, Zi-Jing,Kuang, Liu,Wang, Yu-Xuan,Wang, Bin
supporting information, p. 6344 - 6347 (2017/12/08)
Bromide-mediated intermolecular annulation of phenylethanone derivatives with alkynes has been developed, which allows for the regioselective formation of polysubstituted 1-naphthols. The usage of readily available bromine catalyst, broad substrate scope, and mild conditions make this protocol very practical. Mechanistic investigations reveal that the bromination of phenylethanone derivatives occurs to yield bromo-substituted intermediates, which react in situ with alkynes to furnish the desired 1-naphthols.
