470478-90-1 Usage
Description
4-(4-TERT-BUTOXYCARBONYLPIPERAZINYL)PHENYLBORONIC ACID, PINACOL ESTER is a chemical compound that serves as a key intermediate in the synthesis of various radiolabeled compounds. It is characterized by its ability to form stable boronate esters, which are essential for the development of radiopharmaceuticals.
Uses
Used in Pharmaceutical Industry:
4-(4-TERT-BUTOXYCARBONYLPIPERAZINYL)PHENYLBORONIC ACID, PINACOL ESTER is used as a reactant for the preparation of 211Atand 125I-radiolabeled compounds. These radiolabeled compounds are crucial in the development of targeted radiopharmaceuticals for diagnostic and therapeutic applications in nuclear medicine. 4-(4-TERT-BUTOXYCARBONYLPIPERAZINYL)PHENYLBORONIC ACID, PINACOL ESTER's ability to form stable boronate esters allows for the efficient incorporation of radioactive isotopes, enhancing the effectiveness of these radiopharmaceuticals in detecting and treating various diseases, including cancer.
Used in Radiochemistry Research:
In the field of radiochemistry, 4-(4-TERT-BUTOXYCARBONYLPIPERAZINYL)PHENYLBORONIC ACID, PINACOL ESTER is used as a valuable building block for the synthesis of novel radiotracers. These radiotracers are essential tools in understanding biological processes and developing new therapeutic strategies. 4-(4-TERT-BUTOXYCARBONYLPIPERAZINYL)PHENYLBORONIC ACID, PINACOL ESTER's unique chemical properties enable the design and synthesis of innovative radiotracers with improved targeting and imaging capabilities.
Used in Cancer Research:
4-(4-TERT-BUTOXYCARBONYLPIPERAZINYL)PHENYLBORONIC ACID, PINACOL ESTER plays a significant role in cancer research, particularly in the development of targeted alpha therapy (TAT) agents. These agents utilize alpha-emitting radionuclides, such as 211At, to deliver highly cytotoxic radiation directly to cancer cells, minimizing damage to surrounding healthy tissue. 4-(4-TERT-BUTOXYCARBONYLPIPERAZINYL)PHENYLBORONIC ACID, PINACOL ESTER's ability to form stable boronate esters with radionuclides makes it an essential component in the design and synthesis of TAT agents.
Check Digit Verification of cas no
The CAS Registry Mumber 470478-90-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,0,4,7 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 470478-90:
(8*4)+(7*7)+(6*0)+(5*4)+(4*7)+(3*8)+(2*9)+(1*0)=171
171 % 10 = 1
So 470478-90-1 is a valid CAS Registry Number.
InChI:InChI=1/C21H33BN2O4/c1-19(2,3)26-18(25)24-14-12-23(13-15-24)17-10-8-16(9-11-17)22-27-20(4,5)21(6,7)28-22/h8-11H,12-15H2,1-7H3
470478-90-1Relevant articles and documents
Nucleophilic18F-Labeling of Spirocyclic Iodonium Ylide or Boronic Pinacol Ester Precursors: Advantages and Disadvantages
Petersen, Ida Nymann,Kristensen, Jesper Langgaard,Herth, Matthias Manfred
, p. 453 - 458 (2017)
The field of labeling electron-rich aryl compounds with nucleophilic [18F]fluoride has recently expanded with radiofluorination strategies that apply boronic esters or spirocyclic iodonium ylides as precursors. Herein, we present a direct compa
RET INHIBITORS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF
-
, (2020/07/06)
Provided herein are a RET inhibitor, a pharmaceutical composition thereof and uses thereof. In particular, provided is a compound having Formula (I) or a stereoisomer, a geometric isomer, a tautomer, an N-oxide, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof. Provided is a pharmaceutical composition comprising the compound, and uses of the compound and pharmaceutical composition thereof for the preparation of a medicament, in particular for treatment and prevention of RET-related diseases and conditions, including cancer, irritable bowel syndrome, and/or pain associated with irritable bowel syndrome.
Substituted piperazine compounds and method and use thereof
-
, (2019/03/21)
The invention relates to a new piperazine compound and a drug composition comprising the compound, which are used for inhibiting 5-hydroxytryptamine reuptake and/or agonizing 5-HT1A receptors. The invention also relates to methods for preparing the compou