Phenylboronic Acid Pinacol Ester - ≥98% , CAS No.24388-23-6

CAS: 24388-23-6 Cat. No.: P119610 Peso molecular: 204.07 Beilstein Registry Number: 16(4)1658 Número EC: 629-233-1
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
AKOS015951124 | Phenylboronic acid pinacol ester | 4,4,5,5-tetramethyl-1,3,2-dioxaborolylbenzene | MFCD31699955 | 1872193-24-2 | MFCD00966985 | OSM-S-460 | A817261 | phenylboronic pinacol ester | SY246300 | FT-0728642 | SCHEMBL90476 | phenyl boronic acid
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
P119610-5g
10
9,90US$
25g
P119610-25g
8
21,90US$
100g
P119610-100g
3
81,90US$
500g
P119610-500g
1
385,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Product Introduction

Phenylboronic acid, pinacol ester, also known as boronate ester, is generally used in metal-catalyzed C-C bond formation reactions like Suzuki–Miyaura reaction.


Application

Phenylboronic acid pinacol ester can be used:

To prepare sulfinamide derivatives by reacting with diethylaminosulfur trifluoride (DAST) and potassium phenyltrifluoroborate.

As a substrate in the study of Suzuki–Miyaura coupling of various aryl iodides over SiliaCat Pd(0).

Specifications

Sinónimos
AKOS015951124 | Phenylboronic acid pinacol ester | 4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolylbenzene | MFCD31699955 | 1872193-24-2 | MFCD00966985 | OSM-S-460 | A817261 | phenylboronic pinacol ester | SY246300 | FT-0728642 | SCHEMBL90476 | phenyl boronic acid
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488190355
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488190355
Sonrisas canónicasB1(OC(C(O1)(C)C)(C)C)C2=CC=CC=C2
IUPAC Name4,4,5,5-tetramethyl-2-phenyl-1,3,2-dioxaborolane
InChIKeyKKLCYBZPQDOFQK-UHFFFAOYSA-N
INCHI1S/C12H17BO2/c1-11(2)12(3,4)15-13(14-11)10-8-6-5-7-9-10/h5-9H,1-4H3
Isómeros SMILES B1(OC(C(O1)(C)C)(C)C)C2=CC=CC=C2
WGK Alemania 3
Peso molecular 204.07
Beilstein 16(4)1658
Reaxy-Rn 2937404
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2937404&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzene and substituted derivatives
Alternative Parents Dioxaborolanes  Boronic acid esters  Oxacyclic compounds  Organic metalloid salts  Organooxygen compounds  Organoboron compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Monocyclic benzene moiety - 1,3,2-dioxaborolane - Boronic acid ester - Boronic acid derivative - Oxacycle - Organic metalloid salt - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organoboron compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

15 results found

Lot NumberCertificate TypeFechaArticulo
L2103180Certificate of AnalysisSep 09, 2025 P119610
L2103181Certificate of AnalysisSep 09, 2025 P119610
G2525049Certificate of AnalysisJul 31, 2025 P119610
D2509617Certificate of AnalysisJun 18, 2024 P119610
D2509618Certificate of AnalysisJun 18, 2024 P119610
D2509626Certificate of AnalysisJun 18, 2024 P119610
E2322148Certificate of AnalysisFeb 06, 2023 P119610
E2322163Certificate of AnalysisFeb 06, 2023 P119610
E2322164Certificate of AnalysisFeb 06, 2023 P119610
E2322180Certificate of AnalysisFeb 06, 2023 P119610
E2322185Certificate of AnalysisFeb 06, 2023 P119610
E2322186Certificate of AnalysisFeb 06, 2023 P119610
E2322203Certificate of AnalysisFeb 06, 2023 P119610
K1813240Certificate of AnalysisSep 13, 2022 P119610
C1815210Certificate of AnalysisJan 25, 2022 P119610

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Propiedades químicas y físicas
Punto de inflamación (°F)224.6°F
Punto de inflamación (°C)107℃
Punto de ebullición (°C)130°C/20mmHg
Punto de fusión (°C)28°C
Peso molecular204.080 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass204.132 Da
Monoisotopic Mass204.132 Da
Topological Polar Surface Area18.500 Ų
Heavy Atom Count15
Formal Charge0
Complexity216.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Calculadoras de soluciones
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