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About This Item
Empirical Formula (Hill Notation):
C13H19BO4
CAS Number:
Molecular Weight:
250.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Product Name
4-Hydroxy-3-methoxyphenylboronic acid pinacol ester, 98%
InChI
1S/C13H19BO4/c1-12(2)13(3,4)18-14(17-12)9-6-7-10(15)11(8-9)16-5/h6-8,15H,1-5H3
SMILES string
COc1cc(ccc1O)B2OC(C)(C)C(C)(C)O2
InChI key
WFSJROCEOJANPD-UHFFFAOYSA-N
assay
98%
mp
105-109 °C (lit.)
Quality Level
Related Categories
Application
4-Hydroxy-3-methoxyphenylboronic acid pinacol ester can be used as a reactant:
- In the Suzuki-Miyaura cross-coupling reaction.
- To prepare ethylidenedihydroindolones as potential neoplastic agents.
- To synthesize 5,6-dihydropyrrolo[2,1-b]isoquinoline derivatives, which can be utilized as scaffolds to prepare lamellarin analogs via regioselective bromination and Suzuki cross-coupling reactions.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Synthesis and biological evaluation of 3-ethylidene-1, 3-dihydro-indol-2-ones as novel checkpoint 1 inhibitors
L Nan-Horng, et al.
Bioorganic & Medicinal Chemistry Letters, 16(2), 421-426 (2006)
5, 6-Dihydropyrrolo [2, 1-b] isoquinolines as scaffolds for synthesis of lamellarin analogues
Olsen CA, et al.
Tetrahedron Letters, 46(12), 2041-2044 (2005)
New oxidative labels for electrochemical detection of DNA
Simonova A, et al.
Collection of Czechoslovak Chemical Communications, 14, 365-366 (2015)
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