2-Picoline borane complex - ≥95% , CAS No.3999-38-0

CAS: 3999-38-0 Cat. No.: P122349 Formula: C₆H₇N · BH₃ Peso molecolare: 106.96 Beilstein Registry Number: 20(3/4)2679 Numero EC: 609-767-1 PubChem CID: 11320914

GRADE & PURITY ≥95%

Synonyms

α-picoline borane | 2-Methylpyridineborane | Trihydro(2-methylpyridine)-boron | picoline borane | QHXLIQMGIGEHJP-UHFFFAOYSA-N | 2-Picolin Borane | Borane - 2-Picoline Complex

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Panoramica

2-Methylpyridine borane complex is a nontoxic alternate to the reducing agent sodium cyanoborohydride.

Specifications

Sinonimi

α-picoline borane | 2-Methylpyridineborane | Trihydro(2-methylpyridine)-boron | picoline borane | QHXLIQMGIGEHJP-UHFFFAOYSA-N | 2-Picolin Borane | Borane - 2-Picoline Complex

Specifiche e purezza

≥95%

Applicazione

2-Methylpyridine borane complex solution (2-Picoline borane complex) was used as reducing agent for the labeling of oligosaccharides by reductive amination. It may be used in the following studies: Synthesis of alkoxyamine derivatives, via reduction of ox

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥95%

Nomi e identificatori

Pubchem Sid

508808442

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508808442

Sorrisi canonici

[B].CC1=CC=CC=N1

InChIKey

QHXLIQMGIGEHJP-UHFFFAOYSA-N

INCHI

1S/C6H7N.B/c1-6-4-2-3-5-7-6;/h2-5H,1H3;

Isomeri SMILES

[B].CC1=CC=CC=N1

WGK Germania

3

PubChem CID

11320914

Peso molecolare

106.96

Beilstein

20(3/4)2679

Reaxy-Rn

3679529

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Pyridines and derivatives
      • Subclass Methylpyridines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Pyridines and derivatives
• Subclass: Methylpyridines
• Intermediate Tree Nodes: Not available
• Direct Parent: Methylpyridines
• Alternative Parents: Heteroaromatic compounds Organic metalloid salts Azacyclic compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Methylpyridine - Heteroaromatic compound - Azacycle - Organic metalloid salt - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as methylpyridines. These are organic compounds containing a pyridine ring substituted at one or more positions by a methyl group.
• 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

Proprietà chimiche e fisiche

• Sensibilità: Moisture sensitive
• Punto di infiammabilità (°F): 212 °F
• Punto di infiammabilità (°C): 100 °C
• Punto di fusione (°C): 44-46°C
• Peso molecolare: 103.940 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 104.067 Da
• Monoisotopic Mass: 104.067 Da
• Topological Polar Surface Area: 12.900 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 52.100
• 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: 2

XLogP3