862466-15-7 Usage
Uses
Used in Pharmaceutical Industry:
3-N-BOC-AMINO-3-(3-FLUOROPHENYL)-1-PROPANOL is used as a key intermediate in the synthesis of pharmaceuticals for its ability to enhance the properties of drug molecules. Its incorporation can lead to improved pharmacokinetics, such as increased bioavailability and selectivity, which are crucial for the effectiveness and safety of medications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-N-BOC-AMINO-3-(3-FLUOROPHENYL)-1-PROPANOL is utilized as a precursor in the development of new pesticides and herbicides. 3-N-BOC-AMINO-3-(3-FLUOROPHENYL)-1-PROPANOL's fluorinated nature can impart specific characteristics to these chemicals, such as higher stability and targeted biological activity, which are essential for effective crop protection.
Used in Medicinal Chemistry Research:
3-N-BOC-AMINO-3-(3-FLUOROPHENYL)-1-PROPANOL is employed as a chiral auxiliary in medicinal chemistry research. It aids in the asymmetric synthesis of biologically active molecules, enabling the creation of enantiomerically pure compounds. This is vital for ensuring the desired therapeutic effects and minimizing potential side effects of drugs.
Used in the Development of Synthetic Methodologies:
3-N-BOC-AMINO-3-(3-FLUOROPHENYL)-1-PROPANOL is also used in the advancement of synthetic methodologies, providing a foundation for the creation of innovative chemical processes. Its unique structure allows for the exploration of new reaction pathways and the development of more efficient and selective synthetic routes.
Used in the Production of Fluorinated Organic Compounds:
3-N-BOC-AMINO-3-(3-FLUOROPHENYL)-1-PROPANOL is utilized in the synthesis of fluorinated organic compounds, which have a wide range of applications across various industries. The introduction of fluorine atoms can significantly alter the physical, chemical, and biological properties of organic molecules, making them valuable for applications such as materials science, chemical engineering, and pharmaceutical development.
Check Digit Verification of cas no
The CAS Registry Mumber 862466-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,4,6 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 862466-15:
(8*8)+(7*6)+(6*2)+(5*4)+(4*6)+(3*6)+(2*1)+(1*5)=187
187 % 10 = 7
So 862466-15-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H20FNO3/c1-14(2,3)19-13(18)16-12(7-8-17)10-5-4-6-11(15)9-10/h4-6,9,12,17H,7-8H2,1-3H3,(H,16,18)
862466-15-7Relevant articles and documents
Structure-activity relationships of 1,3,5-triazine-2,4,6-triones as human gonadotropin-releasing hormone receptor antagonists
Guo, Zhiqiang,Wu, Dongpei,Zhu, Yun-Fei,Tucci, Fabio C.,Regan, Collin F.,Rowbottom, Martin W.,Struthers, R. Scott,Xie, Qiu,Reijmers, Shelby,Sullivan, Susan K.,Sai, Yang,Chen, Chen
, p. 3685 - 3690 (2007/10/03)
SAR studies of 1,3,5-triazine-2,4,6-triones as human gonadotropin-releasing hormone receptor antagonists resulted in potent compounds. The best compound from the series had a binding affinity of 2 nM.
