1315552-06-7 Usage
Uses
Used in Pharmaceutical Industry:
C7H10N4O is used as an intermediate in the synthesis of Loline (I707255) for its potential pharmaceutical applications. Loline, an alkaloid isolated from fungal endophytes, has shown promise in various therapeutic areas, making C7H10N4O a valuable compound in the development of new drugs and treatments.
Used in Chemical Synthesis:
C7H10N4O is used as a key intermediate in the synthesis of various organic compounds, particularly those with potential applications in the pharmaceutical, agrochemical, and materials science industries. Its unique molecular structure allows for further functionalization and modification, enabling the creation of a wide range of novel compounds with diverse properties and applications.
Used in Research and Development:
C7H10N4O is used as a research compound for studying the properties and reactivity of similar organic molecules. Its synthesis and characterization can provide valuable insights into the behavior of related compounds, contributing to the advancement of chemical knowledge and the development of new synthetic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 1315552-06-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,5,5 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1315552-06:
(9*1)+(8*3)+(7*1)+(6*5)+(5*5)+(4*5)+(3*2)+(2*0)+(1*6)=127
127 % 10 = 7
So 1315552-06-7 is a valid CAS Registry Number.
1315552-06-7Relevant academic research and scientific papers
An efficient synthesis of loline alkaloids
Cakmak, Mesut,Mayer, Peter,Trauner, Dirk
supporting information; experimental part, p. 543 - 545 (2012/04/04)
Loline (1) is a small alkaloid that, in spite of its simple-looking structure, has posed surprising challenges to synthetic chemists. It has been known for more than a century and has been the subject of extensive biological investigations, but only two total syntheses have been achieved to date. Here, we report an asymmetric total synthesis of loline that, with less then ten steps, is remarkably short. Our synthesis incorporates a Sharpless epoxidation, a Grubbs olefin metathesis and an unprecedented transannular aminobromination, which converts an eight-membered cyclic carbamate into a bromopyrrolizidine. The synthesis is marked by a high degree of chemo- and stereoselectivity and gives access to several members of the loline alkaloid family. It delivers sufficient material to support a programme aimed at studying the complex interactions between plants, fungi, insects and bacteria brokered by loline alkaloids.
