1315552-05-6 Usage
Uses
Used in Pharmaceutical Industry:
C7H11ClN4O is used as an intermediate in the synthesis of Loline (I707255) for its potential applications in the development of new pharmaceutical compounds. As Loline is an alkaloid isolated from fungal endophytes, it may possess unique biological activities that can be harnessed for therapeutic purposes.
Used in Agricultural Industry:
C7H11ClN4O, being a part of the synthesis of Loline, may also find applications in the agricultural industry. Loline and its derivatives could potentially be used as natural pesticides or fungicides, leveraging their bioactive properties to protect crops from pests and diseases.
Used in Chemical Research:
C7H11ClN4O serves as a valuable compound in chemical research, particularly in the study of alkaloids and their derivatives. Its unique structure and properties make it an interesting subject for further investigation, which could lead to the discovery of new chemical reactions, synthesis methods, or applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1315552-05-6 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 1315552-05:
(9*1)+(8*3)+(7*1)+(6*5)+(5*5)+(4*5)+(3*2)+(2*0)+(1*5)=126
126 % 10 = 6
So 1315552-05-6 is a valid CAS Registry Number.
1315552-05-6Relevant articles and documents
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.
