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761446-44-0 1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole C10H17BN2O2

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Tech Data Relevant

1.Certificate Of Analysis (COA)

2..Material Safety Data Sheet (MSDS)

3.Technical Data Sheet(TDS)

4.Route of synthesis (ROS)

5.Nuclear Magnetic Resonance(NMR)

6.Method of Analysis(MOA)

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CBNumber:	CB0414153
Chemical Name:	1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
Molecular Formula:	C10H17BN2O2
Formula Weight:	208.07
CAS No.:	761446-44-0

1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole Basic information

Product Name:	1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
Synonyms:	1-METHYL-4-1H-PYRAZOLEBORONIC ACID, PINACOL ESTER;1-METHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-1H-PYRAZOLE;1-METHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-PYRAZOLE;1-METHYL-1H-PYRAZOLE-4-BORONIC ACID PINACOL ESTER;1-METHYLPYRAZOLE-4-BORONIC ACID PINACOL ESTER;1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole, 97+%;1-Methyl-4-(4,4,5,5-Tetramethy;1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-
CAS:	761446-44-0
MF:	C10H17BN2O2
MW:	208.07
EINECS:
Product Categories:	Organoborons;Pyrazole;Boronic acid;Heterocyclic Building Blocks;Boronate Esters;Boronic Acids and Derivatives;Chemical Synthesis;Heteroaryl Boronate Esters;Organometallic Reagents
Mol File:	761446-44-0.mol

1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole Chemical Properties

mp	59-64 °C(lit.)
storage temp.	Refrigerator (+4°C)
CAS DataBase Reference	761446-44-0(CAS DataBase Reference)

Safety Information

Hazard Codes	Xn,F,Xi
Risk Statements	22-36/37/38
Safety Statements	26-36-37/39
WGK Germany	3
Hazard Note	Irritant/Flammable
HazardClass	IRRITANT

MSDS Information

Provider	Language
SigmaAldrich	English

1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole Usage And Synthesis

Chemical Properties	White to light yellow crystal powde
Usage	Reagent used for• ;Suzuki-Miyaura cross-coupling reactions1,2,3• ;Transesterification reactions4Reagent used for preparation of• ;Aminothiazoles as γ-secretase modulators5• ;Amino-pyrido-indol-carboxamides, as potential JAK2 inhibitors for myeloproliferative disorders therapy6• ;Pyridine derivatives as TGF-β1 and activin A signalling inhibitors7• ;MK-2461 analogs as inhibitors of c-Met kinase for the treatment of cancer8
Usage	suzuki reaction