Iodomethylboronic acid,pinacol ester

• CAS: 70557-99-2
• Catalog Number: ACM70557992
• Category: Other Products
• Molecular Weight: 267.9
• Molecular Formula: C₇H₁₄BIO₂
• Synonyms: 2-(iodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 70557-99-2, AG-G-75502, SureCN3197440, CTK2H4750, MolPort-015-143-419, Iodomethyl boronic acid pinacol ester, Iodomethylboronic acid, pinacol ester,, KB-52701, B-4679, 1,3,2-Dioxaborolane, 2-(iodomethyl)-4,4,5,5-tetramethyl-
• IUPAC Name: 2-(iodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• Canonical SMILES: B1(OC(C(O1)(C)C)(C)C)CI
• InChI Key: UBNNPAYFVZFWPE-UHFFFAOYSA-N
• Exact Mass: 268.01300
• H-Bond Acceptor: 2
• H-Bond Donor: 0

Synthetic Use

Upstream Synthesis Route 1

• 166330-03-6

• 70557-99-2

Reference: [1] Patent: EP2062901, 2009, A1, . Location in patent: Page/Page column 21-22

Upstream Synthesis Route 2

• 76-09-5
• 167967-38-6

• 70557-99-2

Reference: [1] Organic Letters, 2013, vol. 15, # 17, p. 4588 - 4591

Upstream Synthesis Route 3

• 76-09-5
• 75-11-6

• 70557-99-2

Reference: [1] Journal of Organic Chemistry, 2011, vol. 76, # 2, p. 512 - 522

Upstream Synthesis Route 4

• 66080-23-7

• 70557-99-2

Reference: [1]Journal of Organometallic Chemistry,1979,vol. 170,p. 259 - 264

Downstream Synthesis Route 1

• 110-91-8
• 70557-99-2

• 70558-05-3

Reference: [1]Journal of Organometallic Chemistry,1979,vol. 170,p. 259 - 264

Downstream Synthesis Route 2

• 70557-99-2
• 121-69-7

• 70558-03-1

Reference: [1]Journal of Organometallic Chemistry,1979,vol. 170,p. 259 - 264

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