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(2S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)amino)-2-(4-hydroxycyclohexyl)acetic acid

(2S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)amino)-2-(4-hydroxycyclohexyl)acetic acid

(S,E)-10-(tert-butoxycarbonylamino)-1-(9H-fluoren-9-yl)-14,14-dimethyl-3,12-dioxo-2,13-dioxa-4,9,11-triazapentadec-10-ene-5-carboxylic acid

(S,E)-10-(tert-butoxycarbonylamino)-1-(9H-fluoren-9-yl)-14,14-dimethyl-3,12-dioxo-2,13-dioxa-4,9,11-triazapentadec-10-ene-5-carboxylic acid

2-(9,9-dioctyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

$300.00
CAS No.: 302554-81-0
Catalog No.: 101539
Purity: 95%
MF: C35H53BO2
MW: 516.619
Storage: 2-8 degree Celsius
SMILES: CCCCCCCCC1(CCCCCCCC)C2=C(C=CC=C2)C2=C1C=C(C=C2)B1OC(C)(C)C(C)(C)O1
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SKU
101539
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2-(9,9-dioctyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; CAS No.: 302554-81-0; 2-(9,9-dioctyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane falls under ChemShuttle's building blocks for drug discovery. This fluorene and dioxaborolane-substituted compound serves as a valuable intermediate in cross-coupling reactions. As a chemical online mall, ChemShuttle distributes this compound for diverse applications. The dioxaborolane group provides a useful handle for Suzuki-Miyaura coupling reactions. Researchers in pharmaceutical and materials science fields utilize it as a chemical block to construct molecules with specific properties.

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