1582-18-9 Usage
Description
D-2-Amino-1,1,1-Trifluoro-3-(Methyl)Butane is a chemical compound that features an amino group, a trifluoro functional group, and a butane backbone. It is also known by systematic names such as 2-Amino-1,1,1-trifluoro-3-methylbutane and (2S)-2-amino-3-methyl-1,1,1-trifluorobutane. The presence of methyl and butane groups indicates its organic nature, while the trifluoro component highlights the inclusion of three fluorine atoms in its molecular structure. The exact chemical and physical properties or potential applications of this compound are currently unspecified.
Uses
Since the provided materials do not specify the exact applications of D-2-Amino-1,1,1-Trifluoro-3-(Methyl)Butane, it is not possible to list its uses based on the information given. However, given its chemical structure, it may have potential applications in various industries such as pharmaceuticals, chemical manufacturing, or materials science, depending on its properties and reactivity. Further research and experimentation would be required to determine its specific uses and benefits in these or other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1582-18-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,8 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1582-18:
(6*1)+(5*5)+(4*8)+(3*2)+(2*1)+(1*8)=79
79 % 10 = 9
So 1582-18-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H10F3N/c1-3(2)4(9)5(6,7)8/h3-4H,9H2,1-2H3/t4-/m1/s1
1582-18-9Relevant articles and documents
Economical and practical strategies for synthesis of α-trifluoromethylated amines
Jiang,Cheng,Yuan
, p. 2406 - 2408 (2016/05/19)
A powerful approach to synthesize α-trifluoromethylated amines has been developed. The method is operationally simple, broad in substrate scope and amenable to scale-up using trifluoroacetic anhydride. Meanwhile, the strategy not only provided a versatile approach to synthesize α-trifluoromethylated amines but also provides a new method for exploring the new reactivity of trifluoroacetic anhydride.
