120225-79-8 Usage
Description
TERT-BUTYL 3-[4-(2-AMINO-ETHYL)-PHENYL]-PROPIONATE is a chemical compound characterized by its unique structure as a derivative of t-butyl 3-(4-methylphenyl)propionate, featuring an additional aminoethyl group. TERT-BUTYL 3-[4-(2-AMINO-ETHYL)-PHENYL]-PROPIONATE is recognized for its pleasant floral aroma and is utilized in various applications across different industries due to its sweet, fruity scent.
Uses
Used in Fragrance and Flavoring Industry:
TERT-BUTYL 3-[4-(2-AMINO-ETHYL)-PHENYL]-PROPIONATE is used as a synthetic intermediate for enhancing the fragrance and flavor profiles of various products. Its sweet, fruity scent is particularly valued in this industry to create appealing scents for consumer products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, TERT-BUTYL 3-[4-(2-AMINO-ETHYL)-PHENYL]-PROPIONATE serves as a crucial synthetic intermediate. Its role in the synthesis of pharmaceutical compounds highlights its importance in drug development and production.
Used in Cosmetic and Personal Care Products:
TERT-BUTYL 3-[4-(2-AMINO-ETHYL)-PHENYL]-PROPIONATE is used as a fragrance ingredient in the cosmetic and personal care industry. Its ability to impart a pleasant aroma to products such as perfumes, lotions, and creams makes it a valuable component in these formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 120225-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,2 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120225-79:
(8*1)+(7*2)+(6*0)+(5*2)+(4*2)+(3*5)+(2*7)+(1*9)=78
78 % 10 = 8
So 120225-79-8 is a valid CAS Registry Number.
120225-79-8Relevant articles and documents
2-(N'-aralkylidenehydrazino)adenosines: Potent and selective coronary vasodilators
Niiya,Thompson,Silvia,Olsson
, p. 4562 - 4566 (2007/10/02)
This study aimed at the development of 2-(N'- aralkylidenehydrazino)adenosines as coronary vasodilators. The reaction of aromatic aldehydes or ketones with 2-hydrazinoadenosine in refluxing methanol formed the target compounds 2-27 as crystalline products