2-(Methanesulfonylamino)phenylboronic acid pinacol ester - ≥97% , CAS No.380430-60-4

CAS: 380430-60-4 Cat. No.: M170024 Peso molecular: 297.18 Número EC: 626-256-9

GRADE & PURITY ≥97%

Synonyms

AB11227 | 2-METHANESULFONYLAMINOPHENYLBORONIC ACID, PINACOL ESTER | 2-Methylsulfonylaminophenylboronic acid, pinacol ester | AKOS015949582 | SCHEMBL520862 | SY024891 | (2-(METHYLSULFONAMIDO)PHENYL)BORONIC ACID PINACOL ESTER | [(2-Methylsulfonyl)aminopheny

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

AB11227 | 2-METHANESULFONYLAMINOPHENYLBORONIC ACID, PINACOL ESTER | 2-Methylsulfonylaminophenylboronic acid, pinacol ester | AKOS015949582 | SCHEMBL520862 | SY024891 | (2-(METHYLSULFONAMIDO)PHENYL)BORONIC ACID PINACOL ESTER | [(2-Methylsulfonyl)aminopheny

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 488194834
• Sonrisas canónicas: B1(OC(C(O1)(C)C)(C)C)C2=CC=CC=C2NS(=O)(=O)C
• IUPAC Name: N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanesulfonamide
• InChIKey: ADAOINPTCZWNBZ-UHFFFAOYSA-N
• INCHI: 1S/C13H20BNO4S/c1-12(2)13(3,4)19-14(18-12)10-8-6-7-9-11(10)15-20(5,16)17/h6-9,15H,1-5H3
• Isómeros SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC=CC=C2NS(=O)(=O)C
• WGK Alemania: 3
• Peso molecular: 297.18
• Reaxy-Rn: 11253241
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11253241&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Sulfanilides

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Sulfanilides
• Intermediate Tree Nodes: Not available
• Direct Parent: Sulfanilides
• Alternative Parents: Organosulfonamides Organic sulfonamides Dioxaborolanes Boronic acid esters Aminosulfonyl compounds Oxacyclic compounds Organic metalloid salts Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organometalloid compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Sulfanilide - Organic sulfonic acid amide - Organosulfonic acid amide - Boronic acid ester - 1,3,2-dioxaborolane - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Boronic acid derivative - Oxacycle - Organic metalloid salt - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic metalloid moeity - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as sulfanilides. These are organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1.
• 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

• Punto de fusión (°C): 130-134°C
• Peso molecular: 297.200 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 297.121 Da
• Monoisotopic Mass: 297.121 Da
• Topological Polar Surface Area: 73.000 Ų
• Heavy Atom Count: 20
• Formal Charge: 0
• Complexity: 441.000
• 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