1270357-74-8 Usage
Uses
Used in Pharmaceutical Industry:
1-(6-fluoropyridin-2-yl)ethan-1-amine is used as a building block for the development of new pharmaceuticals. Its unique structure allows for the creation of complex organic molecules that can be tailored for specific therapeutic applications, potentially leading to the discovery of novel drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(6-fluoropyridin-2-yl)ethan-1-amine is utilized as a key component in the synthesis of various agrochemicals. Its incorporation into these compounds can enhance their performance, providing more effective pest control and crop protection solutions.
Used in Specialty Chemicals:
1-(6-fluoropyridin-2-yl)ethan-1-amine also finds application in the synthesis of specialty chemicals, where its unique properties can be leveraged to create compounds with specific functions and applications in various industries, such as materials science, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 1270357-74-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,0,3,5 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1270357-74:
(9*1)+(8*2)+(7*7)+(6*0)+(5*3)+(4*5)+(3*7)+(2*7)+(1*4)=148
148 % 10 = 8
So 1270357-74-8 is a valid CAS Registry Number.
1270357-74-8Relevant academic research and scientific papers
Highly enantioselective direct asymmetric reductive amination of 2-acetyl-6-substituted pyridines
Azuma, Kazuki,Yamada, Masatoshi,Yamano, Mitsuhisa
supporting information, p. 3364 - 3367 (2021/05/31)
A highly direct asymmetric reductive amination of a variety of ketone substrates, including 2-acetyl-6-substituted pyridines, β-keto esters, β-keto amides, and 1-(6-methylpyridin-2-yl)propan-2-one, has been disclosed for the first time (94.6% to >99.9% ee). With ammonium trifluoroacetate as the nitrogen source, various chiral corresponding primary amines were prepared in excellent enantioselectivity and conversion in the presence of a commercially available and inexpensive chiral catalyst, Ru(OAc)2{(S)-binap}, under 0.8 MPa of hydrogen gas pressure.
