2-Thiopheneboronic acid MIDA ester

• CAS: 1158984-92-9
• Catalog Number: ACM1158984929
• Category: Other Products
• Molecular Weight: 239.06
• Molecular Formula: C9H10BNO4S
• Synonyms: SureCN13369974, 2-Thiopheneboronic acid MIDA ester, AKOS005166814, 1158984-92-9
• IUPAC Name: 6-methyl-2-thiophen-2-yl-1,3,6,2-dioxazaborocane-4,8-dione
• SMILES: [B-]12([N+](CC(=O)O1)(CC(=O)O2)C)C3=CC=CS3
• InChI Key: WWELVLHUROSDIA-UHFFFAOYSA-N
• Exact Mass: 239.04200
• H-Bond Acceptor: 6
• H-Bond Donor: 0

Synthetic Use

Upstream Synthesis Route 1

• 6165-68-0
• 4408-64-4

• 1158984-92-9

Reference: [1]Knapp, David M.; Gillis, Eric P.; Burke, Martin D.
[Journal of the American Chemical Society, 2009, vol. 131, p. 6961 - 6963]
[2]Current Patent Assignee: UNIVERSITY OF ILLINOIS (SYSTEM) - WO2010/36921, 2010, A2
Location in patent: Page/Page column 35
[3]Xu, Liang; Ding, Siyi; Li, Pengfei
[Angewandte Chemie - International Edition, 2014, vol. 53, # 7, p. 1822 - 1826][Angew. Chem., 2014, vol. 126, # 7, p. 1853 - 1857,5]

Downstream Synthesis Route 1

• 1158984-92-9

• 6165-68-0

Reference: [1] Journal of the American Chemical Society, 2009, vol. 131, p. 6961 - 6963

Downstream Synthesis Route 2

• 1158984-92-9
• 7732-18-5

• 6165-68-0

Reference: [1] Journal of the American Chemical Society, 2009, vol. 131, p. 6961 - 6963

Downstream Synthesis Route 3

• 1158984-92-9
• 7732-18-5

• 6165-68-0

Reference: [1]Knapp, David M.; Gillis, Eric P.; Burke, Martin D.
[Journal of the American Chemical Society, 2009, vol. 131, p. 6961 - 6963]

Downstream Synthesis Route 4

• 1448-87-9
• 1158984-92-9

• 40353-41-1

Reference: [1]Knapp, David M.; Gillis, Eric P.; Burke, Martin D.
[Journal of the American Chemical Society, 2009, vol. 131, p. 6961 - 6963]

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