68384-70-3 Usage
Uses
Used in Food and Beverage Industry:
Ethyl 3-(methylamino)butanoate is utilized as a flavoring agent to enhance the taste and aroma of various food and beverage products. Its sweet, fruity scent allows it to contribute a tropical or fruity note, making it a popular choice for manufacturers aiming to create appealing and distinctive flavors in their offerings.
Used in Consumer Goods Production:
Beyond its applications in the food and beverage sector, ethyl 3-(methylamino)butanoate is also employed in the production of a range of consumer goods. Its versatility as a flavoring agent makes it suitable for use in products such as perfumes, cosmetics, and other fragranced items, where its sweet and fruity characteristics can provide a pleasant and attractive scent profile.
Check Digit Verification of cas no
The CAS Registry Mumber 68384-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,8 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 68384-70:
(7*6)+(6*8)+(5*3)+(4*8)+(3*4)+(2*7)+(1*0)=163
163 % 10 = 3
So 68384-70-3 is a valid CAS Registry Number.
68384-70-3Relevant academic research and scientific papers
Inhibitors of serotonin reuptake
-
, (2008/06/13)
This invention provides compounds and a method for the inhibition of serotonin reuptake in mammals.
Chemo- and diastereoselective reduction of β-enamino esters: A convenient synthesis of both cis- and trans-γ-amino alcohols and β-amino esters
Bartoli,Cimarelli,Marcantoni,Palmieri,Petrini
, p. 5328 - 5335 (2007/10/02)
Convenient procedures for the chemo- and diastereoselective reduction of b-enamino esters 1 are described. Both cis- and trans-γ-amino alcohols 2 or b-amino esters 3 can be prepared by reduction of b-enamino esters 1, readily available starting materials, with the use of inexpensive reagents Na/i-PrOH or NaHB(OAc)3/AcOH, respectively, and the appropriate reduction conditions. The mechanisms and diastereoselectivities for the reductions are discussed. The relative configurations and conformations of the diastereoisomeric γ-amino alcohols 2 and β-amino esters 3 obtained are established by 1H and 13C NMR study and unequivocally set by their cyclic derivatives tetrahydro-1,3-oxazines 4.
