Ester pinacol del ácido isopropilborónico - ≥98% , CAS No.76347-13-2

CAS: 76347-13-2 Cat. No.: I139251 Peso molecular: 170.06 Número EC: 878-705-5

GRADE & PURITY ≥98%

Synonyms

2-isopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | C9H19BO2 | AKOS006344208 | DTXSID50508223 | Isopropyl pinacolato boronate | MFCD05663856 | BS-2076 | 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1-methylethyl)- | 2-ISOPROPYLBORONIC ACID, PINACOL ESTER

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinónimos

2-isopropyl-4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolane | C9H19BO2 | AKOS006344208 | DTXSID50508223 | Isopropyl pinacolato boronate | MFCD05663856 | BS-2076 | 1, 3, 2-Dioxaborolane, 4, 4, 5, 5-tetramethyl-2-(1-methylethyl)- | 2-ISOPROPYLBORONIC ACID, PINACOL ESTER

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488198233
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488198233
• Sonrisas canónicas: B1(OC(C(O1)(C)C)(C)C)C(C)C
• IUPAC Name: 4,4,5,5-tetramethyl-2-propan-2-yl-1,3,2-dioxaborolane
• InChIKey: MECCSFDHAVAAAW-UHFFFAOYSA-N
• INCHI: 1S/C9H19BO2/c1-7(2)10-11-8(3,4)9(5,6)12-10/h7H,1-6H3
• Isómeros SMILES: B1(OC(C(O1)(C)C)(C)C)C(C)C
• Peso molecular: 170.06
• Reaxy-Rn: 6917388
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6917388&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 Monoalkylboranes Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: 1,3,2-dioxaborolane - Boronic acid ester - Oxacycle - Organic metalloid salt - Organoheterocyclic compound - Organic oxygen compound - Monoalkylborane - Alkylborane - 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: Moisture Sensitive
• Índice de refracción: 1.41
• Punto de inflamación (°C): 57 °C
• Peso molecular: 170.060 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 170.148 Da
• Monoisotopic Mass: 170.148 Da
• Topological Polar Surface Area: 18.500 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 159.000
• 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