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Structure

1H-Indole,6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

CAS
642494-36-8
Catalog Number
ACM642494368
Category
Other Products
Molecular Weight
243.11
Molecular Formula
C14H18BNO2

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Specification

Synonyms
642494-36-8, Indole-6-boronic acid pinacol ester, 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole, Indole-6-boronicacidpinacolester, Indole-6-boronic acid pinacolate, Indole-6-boronic acid, pinacol ester, PubChem23558, SureCN13718, CTK8B3119, MolPort-002-041-536, ANW-41798, AKOS015950894, PB27777, AK-77116, KB-44243, AB1005668, A8818, AM20040947, 1H-INDOLE-6-BORONIC ACID PINACOL ESTER, 3-hydroxy-2,3-dimethylbutan-2-yl hydrogen 1H-indol-6-ylboronate
IUPAC Name
6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
Canonical SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CC3=C(C=C2)C=CN3
InChI Key
VNDFXJNIKZCQRY-UHFFFAOYSA-N
Boiling Point
395.997ºC at 760 mmHg
Density
1.112 g/cm³
Exact Mass
243.14300
H-Bond Acceptor
2
H-Bond Donor
1
Safety Description
26-36/37/39

Upstream Synthesis Route 1

  • 52415-29-9
  • 73183-34-3
  • 642494-36-8

Reference: [1] Journal of the American Chemical Society, 2017, vol. 139, # 24, p. 8267 - 8276

Upstream Synthesis Route 2

  • 399-51-9
  • 25015-63-8
  • 642494-36-8

Reference: [1] Organic Letters, 2018,

Upstream Synthesis Route 3

  • 52415-29-9
  • 25015-63-8
  • 120-72-9
  • 642494-36-8

Reference: [1] Organic Letters, 2014, vol. 16, # 9, p. 2366 - 2369

Upstream Synthesis Route 4

  • 52415-29-9
  • 73183-34-3
  • 642494-36-8

Reference: [1]Journal of the American Chemical Society,2017,vol. 139,p. 8267 - 8276

Upstream Synthesis Route 5

  • 104-92-7
  • 777061-38-8
  • 642494-36-8
  • 147621-14-5

Reference: [1]Journal of Organic Chemistry,2004,vol. 69,p. 6812 - 6820

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