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725323 Sigma-Aldrich

1-Methyl-1H-indazole-4-boronic acid pinacol ester

97%

  • CAS Number 885698-94-2

  • Empirical Formula (Hill Notation) C14H19BN2O2

  • Molecular Weight 258.12

  •  MDL number MFCD10700158

  •  PubChem Substance ID 329764147

  •  NACRES NA.22

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Properties

Related Categories Boronate Esters, Boronic Acids and Derivatives, Chemical Synthesis, Heteroaryl Boronate Esters, Organometallic Reagents More...
assay   97%
mp   84-89 °C
storage temp.   2-8°C
SMILES string   Cn1ncc2c(cccc12)B3OC(C)(C)C(C)(C)O3
InChI   1S/C14H19BN2O2/c1-13(2)14(3,4)19-15(18-13)11-7-6-8-12-10(11)9-16-17(12)5/h6-9H,1-5H3
InChI key   OZHFBNULPUBRJF-UHFFFAOYSA-N

Description

Packaging

1 g in glass bottle

250 mg in amber glass bottle

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Protocols & Articles

Articles

Boronic Acid Esters - Chemfiles Volume 4 Article 2

The synthesis of biaryl compounds via the Suzuki–Miyaura coupling reaction has become more commonplace now that many arylboronic acids are readily available. Several years ago, Miyaura et al. demonst...
Chemfiles Volume 4 Article 2
Keywords: Coupling reactions, Suzuki-Miyaura coupling

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Indoles, Purines, and Their Isosteres

Substituted indoles and purines have frequently been referred to as “privileged structures” since they are capable of binding to multiple receptors with high affinity, and thus have applications acro...
Keywords: Building blocks, Medicinal chemistry

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