120811-32-7 Usage
Uses
Used in Pharmaceutical Industry:
2H-PYRAN-3-AMINE, TETRAHYDROis used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form diverse chemical structures and exhibit biological activity. Its presence in drug molecules can contribute to their therapeutic effects and pharmacological properties.
Used in Agrochemical Industry:
In the agrochemical industry, 2H-PYRAN-3-AMINE, TETRAHYDROis utilized as a precursor in the development of agrochemicals, such as pesticides and herbicides. Its reactivity allows for the creation of compounds with specific target activities, enhancing crop protection and yield.
Used in Organic Synthesis:
2H-PYRAN-3-AMINE, TETRAHYDROserves as a versatile building block in organic synthesis, enabling the construction of complex organic molecules with potential applications in various fields, including materials science, fragrances, and dyes.
Used in Medicinal Chemistry:
In medicinal chemistry, 2H-PYRAN-3-AMINE, TETRAHYDROis employed as a structural component in the design and synthesis of new drug candidates. Its unique properties and reactivity contribute to the discovery of novel therapeutic agents with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 120811-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,8,1 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 120811-32:
(8*1)+(7*2)+(6*0)+(5*8)+(4*1)+(3*1)+(2*3)+(1*2)=77
77 % 10 = 7
So 120811-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO/c6-5-2-1-3-7-4-5/h5H,1-4,6H2
120811-32-7Relevant academic research and scientific papers
Direct Access to Primary Amines from Alkenes by Selective Metal-Free Hydroamination
Du, Yi-Dan,Chen, Bi-Hong,Shu, Wei
supporting information, p. 9875 - 9880 (2021/03/29)
Direct and selective synthesis of primary amines from easily available precursors is attractive yet challenging. Herein, we report the rapid synthesis of primary amines from alkenes via metal-free regioselective hydroamination at room temperature. Ammonium carbonate was used as ammonia surrogate for the first time, allowing for efficient conversion of terminal and internal alkenes into linear, α-branched, and α-tertiary primary amines under mild conditions. This method provides a straightforward and powerful approach to a wide spectrum of advanced, highly functionalized primary amines which are of particular interest in pharmaceutical chemistry and other areas.
