1-Boc-6-bromo-indole-2-boronic acid

• CAS: 1217500-59-8
• Catalog Number: ACM1217500598
• Category: Other Products
• Molecular Weight: 340.0
• Molecular Formula: C₁₃H₁₅BBrNO₄
• Synonyms: 1217500-59-8, 1-BOC-6-Bromo-indole-2-boronic acid, (6-Bromo-1-(tert-butoxycarbonyl)-1H-indol-2-yl)boronic acid, ACMC-209afb, CTK4B2633, MolPort-015-142-805, ANW-17781, AKOS015836483, AG-L-20978, AK-91827, BD230000, KB-11518, QC-10932, A-3797, I04-1903, 6-bromo-1-(tert-butoxycarbonyl)-1H-indol-2-ylboronic acid
• IUPAC Name: [6-bromo-1-[(2-methylpropan-2-yl)oxycarbonyl]indol-2-yl]boronic acid
• Canonical SMILES: B(C1=CC2=C(N1C(=O)OC(C)(C)C)C=C(C=C2)Br)(O)O
• InChI Key: RMYFCWUHNRAJJC-UHFFFAOYSA-N
• Exact Mass: 339.02800
• H-Bond Acceptor: 4
• H-Bond Donor: 2

Synthetic Use

Upstream Synthesis Route 1

• 147621-26-9

• 1217500-59-8

Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 6, p. 1852 - 1856

Upstream Synthesis Route 2

• 52415-29-9

• 1217500-59-8

Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 6, p. 1852 - 1856

Upstream Synthesis Route 3

• 34619-03-9

• 1217500-59-8

Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 6, p. 1852 - 1856

Upstream Synthesis Route 4

• 147621-26-9

• 1217500-59-8

Reference: [1]Location in patent: scheme or table
Herdemann, Matthias; Weber, Alexander; Jonveaux, Jérôme; Schwoebel, Frank; Stoeck, Michael; Heit, Isabelle
[Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 6, p. 1852 - 1856]

Downstream Synthesis Route 1

• 1217500-59-8
• 290368-00-2

• 1294514-45-6

Reference: [1]Bioorganic and Medicinal Chemistry Letters,2011,vol. 21,p. 1852 - 1856

Downstream Synthesis Route 2

• 1123-99-5
• 1217500-59-8

• 1572178-12-1

Reference: [1]Bioorganic and Medicinal Chemistry,2014,vol. 22,p. 1708 - 1725

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