642606
trans-3-Phenyl-1-propen-1-ylboronic acid
≥95%
Synonym(s):
trans-3-phenylpropen-1-yl-boronic acid
Sign In to View Organizational & Contract Pricing.
Select a Size
Pricing and availability is not currently available.
About This Item
Empirical Formula (Hill Notation):
C9H11BO2
CAS Number:
Molecular Weight:
161.99
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Skip To
Product Name
trans-3-Phenyl-1-propen-1-ylboronic acid, ≥95%
InChI
1S/C9H11BO2/c11-10(12)8-4-7-9-5-2-1-3-6-9/h1-6,8,11-12H,7H2/b8-4+
SMILES string
[H]\C(Cc1ccccc1)=C(\[H])B(O)O
InChI key
GMGWFDHLFMBIDS-XBXARRHUSA-N
assay
≥95%
form
solid
functional group
phenyl
Quality Level
Related Categories
1 of 4
This Item | 499978 | 576638 | 648787 |
|---|---|---|---|
| assay ≥95% | assay ≥95% | assay ≥95.0% | assay ≥95% |
| form solid | form - | form - | form powder |
| functional group phenyl | functional group - | functional group - | functional group - |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
![Benzo[b]thien-2-ylboronic acid ≥95%](/deepweb/assets/sigmaaldrich/product/structures/251/077/d0ead874-b533-4dcb-890d-8816a0018ccd/640/d0ead874-b533-4dcb-890d-8816a0018ccd.png)
Application
Reactant involved in:
- Carbonylative arylation of allenols
- Oxidative cross-coupling with (trifluoromethyl)trimethylsilane
- Suzuki-Miyaura coupling reactions
- three-component reductive coupling with alkynes
- Enantioselective conjugation to vinyl 2-pyridylsulfones
Other Notes
Contains varying amounts of anhydride
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Ioan-Adrian Stoian et al.
Biosensors & bioelectronics, 155, 112098-112098 (2020-02-25)
A highly selective and sensitive molecularly imprinted polymer (MIP)-based electrochemical sensor was fabricated for the determination of azithromycin, a broad-spectrum macrolide antibiotic, from various biological samples (urine, tears, plasma). The reversible boronate ester bond-mediated, thin (~75 nm) MIP-based biomimetic recognition layer
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service