Allenylboronic Acid Pinacol Ester - ≥95% , CAS No.865350-17-0

CAS: 865350-17-0 Cat. No.: A151404 Peso molecular: 166.03

GRADE & PURITY ≥95%

Synonyms

SY057276 | AMY1622 | C9H15BO2 | AKOS015893166 | 2-Allenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | 4,4,5,5-Tetramethyl-2-(1,2-propadienyl)-1,3,2-dioxaborolane | S10937 | SCHEMBL14725364 | FS-5745 | 1,2-Propadieneboronic Acid Pinacol Ester | MFCD09265121

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

SY057276 | AMY1622 | C9H15BO2 | AKOS015893166 | 2-Allenyl-4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolane | 4, 4, 5, 5-Tetramethyl-2-(1, 2-propadienyl)-1, 3, 2-dioxaborolane | S10937 | SCHEMBL14725364 | FS-5745 | 1, 2-Propadieneboronic Acid Pinacol Ester | MFCD09265121

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥95%

Nombres e identificadores

• Sonrisas canónicas: B1(OC(C(O1)(C)C)(C)C)C=C=C
• InChIKey: CJAOMXUZZONOSD-UHFFFAOYSA-N
• INCHI: 1S/C9H15BO2/c1-6-7-10-11-8(2,3)9(4,5)12-10/h7H,1H2,2-5H3
• Isómeros SMILES: B1(OC(C(O1)(C)C)(C)C)C=C=C
• WGK Alemania: 3
• Peso molecular: 166.03
• Reaxy-Rn: 10152636
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10152636&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Boronic acid derivatives
      • Subclass Boronic acid esters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Boronic acid derivatives
• Subclass: Boronic acid esters
• Intermediate Tree Nodes: Not available
• Direct Parent: Boronic acid esters
• Alternative Parents: Dioxaborolanes Oxacyclic compounds Organic metalloid salts Organooxygen compounds Organometalloid compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: 1,3,2-dioxaborolane - Boronic acid ester - Oxacycle - Organic metalloid salt - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organic metalloid moeity - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as boronic acid esters. These are compounds comprising the boronic acid ester functional group RN(X)OR' (R,R'=alkyl, aryl; X= any O, N, Hal residue).
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Sensibilidad: Air & heat & Moisture sensitive
• Índice de refracción: 1.46
• Punto de inflamación (°F): 149 °F
• Punto de inflamación (°C): 65 °C
• Punto de ebullición (°C): 81 °C/18.6 mmHg
• Peso molecular: 166.030 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 166.117 Da
• Monoisotopic Mass: 166.117 Da
• Topological Polar Surface Area: 18.500 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 211.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

XLogP3