1093819-50-1

1093819-50-1 - Names and Identifiers

Name	1H-Pyrazolo[3,4-b]pyridine-5-boronic acid pinacol ester
Synonyms	1H-Pyrazolo[3,4-B]pyridin... 1H-Pyrazolo[3,4-b]pyridin-5-ylboronic acid pina 1H-Pyrazolo[3,4-B]pyridine-5-boronic acid pinacol 1H-Pyrazolo3,4-bpyridine-boronic acid picol ester 1H-Pyrazol[3,4b]pyridine-5-boronic acid pinacol ester 1H-Pyrazolo[3,4-b]pyridine-boronic acid pinacol ester 1H-Pyrazolo[3,4-B]pyridine-boronic acid pinacol ester 1H-Pyrazolo[3,4-B]pyridine-5-boronic acid pinacol ester 1H-Pyrazolo[3,4-b]pyridine-5-boronic acid pinacol ester 3H-Pyrazolo[3,4-b]pyridine-5-boronic acid pinacol ester 1H-Pyrazolo(3,4-B)pyridine-5-boronic acid pinacol ester 5-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazolo[3,4-B]pyridine 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazolo[3,4-B]pyridine 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazolo[3,4-b]pyridine 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazolo[3,4-b]pyridine 5-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazolo[3,4-B]pyridine 1H-Pyrazolo[3,4-b]pyridine, 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS	1093819-50-1
InChI	InChI=1S/C12H16BN3O2/c1-11(2)12(3,4)18-13(17-11)9-5-8-6-15-16-10(8)14-7-9/h5-7H,1-4H3,(H,14,15,16)

1093819-50-1 - Physico-chemical Properties

Molecular Formula	C12H16BN3O2
Molar Mass	245.09
Density	1.19
Boling Point	415℃
Flash Point	205℃
pKa	9.92±0.40(Predicted)
Storage Condition	under inert gas (nitrogen or Argon) at 2-8°C
Sensitive	Irritant
MDL	MFCD09832892

1093819-50-1 - Introduction

1H-Pyrazolo [3,4-b] pyridine-5-boronic acid pinacol ester, also known as Bpin-F, is an organic compound. The following is a description of its nature, use, preparation and safety information:

Nature:
1H-Pyrazolo [3,4-b] pyridine-5-boronic acid pinacol ester is a colorless to pale yellow solid. It has good solubility and is soluble in common organic solvents.

Use:
1H-Pyrazolo [3,4-b] pyridine-5-boronic acid pinacol ester is an important organic synthesis intermediate. It is widely used in the field of chemical synthesis, and can be used to construct organic molecules containing boron compounds, such as the synthesis of drugs, dyes and polymers.

Preparation Method:
The preparation of 1H-pyrazolo [3,4-b] pyridine-5-boronic acid pinacol ester usually uses organic synthesis reaction. One commonly used method is synthesis by imidazole-catalyzed transesterification of boronic acid with pinacol.

Safety Information:
No specific safety information regarding 1H-pyrazolo [3,4-b] pyridine-5-boronic acid pinacol ester has been reported. However, like most chemicals, they should be used and stored correctly, avoiding contact with skin, eyes and mucous membranes. In case of accidental contact, rinse immediately with water and seek medical help. In addition, when used in the laboratory, care should be taken to comply with relevant operating procedures and safe operating requirements.

Last Update：2024-04-09 21:54:55