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4-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]morpholine

Catalog NumberACM364794809-1

CAS Number364794-80-9

CategorySalt

4-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]morpholine
Synonyms
364794-80-9, 4-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]morpholine, SBB052547, 3-(4-Methylmorpholine)benzeneboronic acid, pinacol ester, 3-(Morpholin-4-ylmethyl)benzeneboronic acid, pinacol ester, 4,4,5,5-tetramethyl-2-[3-(morpholin-4-ylmethyl)phenyl]-1,3,2-dioxaborolane, 4-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)morpholine, AC1MDTP1, SureCN585841, AMTB039, CTK6B2368, MolPort-000-141-064, ANW-28427, AKOS015999576, AG-C-00992, PB20970, QC-4721, RP06843, 4-[[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]morpholine, AK-84225
IUPAC Name
4-[[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]morpholine
Molecular Weight
303.2
Molecular Formula
C17H26BNO3
Canonical SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CC(=CC=C2)CN3CCOCC3
InChI Key
RCGRLLZELIIKDH-UHFFFAOYSA-N
Boiling Point
409.3ºC at 760mmHg
Melting Point
47ºC
Flash Point
201.4ºC
Purity
98
Density
1.08g/cm³
Application
4-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]morpholine serves multiple purposes in advanced chemical synthesis. Primarily, it acts as a reactant in palladium-catalyzed Suzuki-Miyaura coupling reactions, facilitating the creation of biaryl derivatives. This product is also instrumental in synthesizing morpholinylphenyl anilinoquinazoline lapatinib analogs. Additionally, it contributes to the formation of diaryl or heteroaryl triazole quinuclidine derivatives, which are explored as potent α7 nicotinic acetylcholine receptor ligands.
Exact Mass
303.20100
Hazard Statements
C: Corrosive;
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