1H-Isoindole-1,3(2H)-dione,2-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]-

• CAS: 138500-87-5
• Catalog Number: ACM138500875
• Category: Other Products
• Molecular Weight: 363.21
• Molecular Formula: C₂₁H₂₂BNO₄
• Synonyms: ALBB-009359, P5052G1, (4-Phthalimidomethylphenyl)boronic acid pinacol ester, 2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-1H-isoindole-1,3(2H)-dione, 138500-87-5
• IUPAC Name: 2-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]isoindole-1,3-dione
• Canonical SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C=C2)CN3C(=O)C4=CC=CC=C4C3=O
• InChI Key: ZLSIUDAKDAXZRV-UHFFFAOYSA-N
• Boiling Point: 504ºC at 760mmHg
• Melting Point: 155-158ºC
• Flash Point: 258.6ºC
• Density: 1.23g/cm³
• Exact Mass: 363.16400
• Hazard Statements: Xi
• H-Bond Acceptor: 4
• H-Bond Donor: 0

Synthetic Use

Upstream Synthesis Route 1

• 1074-82-4
• 138500-85-3

• 138500-87-5

Reference: [1]Ramalingam, Kondareddiar; Nowotnik, David P.
[Organic Preparations and Procedures International, 1991, vol. 23, # 6, p. 729 - 734]
[2]Chen, Zhaohang; Zhou, Pengcheng; Guo, Yuanxia; Anna, None; Bai, Jiakun; Qiao, Renzhong; Li, Chao
[Journal of Organic Chemistry, 2022, vol. 87, # 5, p. 2624 - 2631]

Downstream Synthesis Route 1

• 138500-87-5

• 138500-88-6

Reference: [1]Molecules,2013,vol. 18,p. 12346 - 12367
[2]Organic Preparations and Procedures International,1991,vol. 23,p. 729 - 734
[3]Patent: WO2006/81807,2006,A2 .Location in patent: Page/Page column 20; 32-33

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