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  • 692735 - 1H-Indazole-6-boronic acid pinacol ester

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692735 Sigma-Aldrich

1H-Indazole-6-boronic acid pinacol ester

≥95%

Synonym: 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole

  • CAS Number 937049-58-6

  • Empirical Formula (Hill Notation) C13H17BN2O2

  • Molecular Weight 244.10

  •  MDL number MFCD07368067

  •  PubChem Substance ID 329761523

  •  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   ≥95%
mp   134-139 °C
storage temp.   room temp
SMILES string   CC1(C)OB(OC1(C)C)c2ccc3cn[nH]c3c2
InChI   1S/C13H17BN2O2/c1-12(2)13(3,4)18-14(17-12)10-6-5-9-8-15-16-11(9)7-10/h5-8H,1-4H3,(H,15,16)
InChI key   YDWZPHAJTNZBEG-UHFFFAOYSA-N

Description

Packaging

1, 5 g in glass bottle

Safety & Documentation

Safety Information

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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