1-Boc-indole-3-boronic acid,pinacol ester

• CAS: 942070-45-3
• Catalog Number: ACM942070453
• Category: Other Products
• Molecular Weight: 343.2
• Molecular Formula: C₁₉H₂₆BNO₄
• Synonyms: 942070-45-3, TERT-BUTYL 3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-INDOLE-1-CARBOXYLATE, SureCN1054068, CTK5H5798, MolPort-015-143-922, ANW-53538, AKOS015999320, AG-H-88343, AM80919, AK-91913, BD230086, KB-11548, 1-BOC-indole-3-boronic acid pinacol ester, 1-BOC-indole-3-boronic acid, pinacol ester, A-3816, 1H-Indole-1-carboxylic acid, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester
• IUPAC Name: tert-butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indole-1-carboxylate
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CN(C3=CC=CC=C23)C(=O)OC(C)(C)C
• InChI Key: WWMZOMHUEMTTQO-UHFFFAOYSA-N
• Exact Mass: 343.19500
• H-Bond Acceptor: 4
• H-Bond Donor: 0

Synthetic Use

Upstream Synthesis Route 1

• 73183-34-3

• 942070-45-3

Reference: [1] Patent: US2011/15232, 2011, A1, . Location in patent: Page/Page column 42-44

Upstream Synthesis Route 2

• 75400-67-8
• 25015-63-8

• 942070-45-3

Reference: [1] Organometallics, 2014, vol. 33, # 13, p. 3514 - 3522
[2] Journal of Organic Chemistry, 2009, vol. 74, # 23, p. 9199 - 9201

Upstream Synthesis Route 3

• 61676-62-8
• 192189-07-4

• 942070-45-3

Reference: [1] Organic Letters, 2013, vol. 15, # 6, p. 1346 - 1349

Upstream Synthesis Route 4

• 75400-67-8
• 25015-63-8

• 942070-45-3

Reference: [1]Organometallics,2014,vol. 33,p. 3514 - 3522
[2]Journal of Organic Chemistry,2009,vol. 74,p. 9199 - 9201

Downstream Synthesis Route 1

• 942070-45-3

• 937366-54-6

Reference: [1]Journal of Organic Chemistry,2009,vol. 74,p. 9199 - 9201

* For details of the synthesis route, please refer to the original source to ensure accuracy.