Description
Tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (CAS: 850568-72-8) is a high-purity boronic ester derivative widely used in organic synthesis and pharmaceutical research. This compound features a pinacol boronate ester group attached to a tert-butyl benzoate moiety, making it an excellent intermediate for Suzuki-Miyaura cross-coupling reactions. With the molecular formula C17H25BO4, it offers exceptional stability and reactivity for constructing complex aromatic systems. Ideal for researchers in medicinal chemistry and material science, this product is rigorously tested for quality and consistency. Available in various quantities to suit laboratory-scale or industrial applications.
Properties
- CAS Number: 850568-72-8
- Complexity: 401
- IUPAC Name: tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
- InChI: InChI=1S/C17H25BO4/c1-15(2,3)20-14(19)12-8-10-13(11-9-12)18-21-16(4,5)17(6,7)22-18/h8-11H,1-7H3
- InChI Key: GNXLDEFJAZGNCJ-UHFFFAOYSA-N
- Exact Mass: 304.1845894
- Molecular Formula: C17H25BO4
- Molecular Weight: 304.2
- SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C=C2)C(=O)OC(C)(C)C
- Topological: 44.8
- Monoisotopic Mass: 304.1845894
- Synonyms: 850568-72-8, Tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate, 4-(tert-Butoxycarbonyl)phenylboronic acid pinacol ester, 4-(TERT-BUTOXYCARBONYL)PHENYLBORONIC ACID, PINACOL ESTER, MFCD03453055, 4-(tert-Butoxycarbonyl)benzeneboronic acid pinacol ester, tert-butyl 4-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate, GNXLDEFJAZGNCJ-UHFFFAOYSA-N, 4-(Boc-)-phenylboronic acid, SCHEMBL900346, DTXSID20402582, (4-(TERT-BUTOXYCARBONYL)PHENYL)BORONIC ACID PINACOL ESTER, BCP11508, AKOS015950765, 4-Boc-phenylboronic Acid Pinacol Ester, CS-W012104, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid tert-butyl ester, DS-16076, SY056873, B5132, EN300-7372455, 4-Tert-butoxycarbonylphenylboronic acid pinacol ester, Z1741981029, 4-(tert-Butoxycarbonyl)phenylboronic acid, pinacol ester, AldrichCPR, 2-(4-tert-Butoxycarbonylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, Tert-butyl4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate, 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzoic acid tert-butyl ester, 4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-Benzoic Acid 1,1-Dimethylethyl Ester
This compound is primarily used as a key intermediate in Suzuki-Miyaura cross-coupling reactions to synthesize biaryl compounds. It is valuable in pharmaceutical research for creating drug candidates with aromatic scaffolds. Additionally, it serves as a building block in material science for developing advanced polymers and OLED materials. Its stability under various conditions makes it suitable for multi-step synthetic routes.
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