| Identification | Back Directory | [Name]
1-Phenylvinylboronic acid | [CAS]
14900-39-1 | [Synonyms]
RARECHEM AH PB 0200
Styrene α-boronic acid
a-Phenylvinylboronic acid
1-PHENYLVINYLBORONIC ACID
Alpha-Phenyl Vinylboronic
α-phenyl vinylboronic acid
1-Phenylvinylboronic acid 95%
(1-Phenylethenyl)boronic acid
(1-Phenylvinyl)boronicacid95%
ALPHA-PHENYL VINYLBORONIC ACID
α-Methylene-α-tolueneboronic acid
Boronic acid, B-(1-phenylethenyl)- | [Molecular Formula]
C8H9BO2 | [MDL Number]
MFCD01074578 | [MOL File]
14900-39-1.mol | [Molecular Weight]
147.97 |
| Chemical Properties | Back Directory | [Melting point ]
125 °C (dec.) (lit.) | [Boiling point ]
321.1±35.0 °C(Predicted) | [density ]
1.090±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [form ]
solid | [pka]
8.98±0.43(Predicted) | [color ]
white | [InChI]
InChI=1S/C8H9BO2/c1-7(9(10)11)8-5-3-2-4-6-8/h2-6,10-11H,1H2 | [InChIKey]
YJCPVMYUISTDKG-UHFFFAOYSA-N | [SMILES]
B(C(C1=CC=CC=C1)=C)(O)O |
| Hazard Information | Back Directory | [Uses]
Reactant involved in:
- Halogenation of alkynes for preparation of enol esters
- Liebeskind-Srogl cross-coupling
- Homocoupling of arylboronic acids for synthesis of biaryls
- Iterative cross-coupling of boronate building blocks
- Enantioselective hydrogenation of hydroxyphenyl styrenes
- Samarium diiodide-mediated cyclization for synthesis of substituted benzannulated cyclooctanol derivatives
- Suzuki-Miyaura cross-coupling for synthesis of C-6-substituted uridine phosphonates
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J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
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https://www.jkchemical.com |
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Energy Chemical
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400-0056266 |
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www.energy-chemical.com |
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AllyChem Co., Ltd.
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0411-62313318 13889470786 |
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www.chemicalbook.com/showsupplierproductslist677/0_en.htm |
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Sigma-Aldrich
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021-61415566 800-8193336 |
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https://www.sigmaaldrich.cn |
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