1,2-Bis(dicyclohexylphosphino)ethane - ≥98% , CAS No.23743-26-2

CAS: 23743-26-2 Cat. No.: B115614 Peso molecular: 422.61 Número EC: 684-243-3

GRADE & PURITY ≥98%

Synonyms

Dcype | Ethylenebis(dicyclohexylphosphine) | dicyclohexyl(2-dicyclohexylphosphanylethyl)phosphane | 1,2-Ethanediylbis[dicyclohexyl]phosphine

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinónimos

Dcype | Ethylenebis(dicyclohexylphosphine) | dicyclohexyl(2-dicyclohexylphosphanylethyl)phosphane | 1, 2-Ethanediylbis[dicyclohexyl]phosphine

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488190174
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488190174
• Sonrisas canónicas: C1CCC(CC1)P(CCP(C2CCCCC2)C3CCCCC3)C4CCCCC4
• IUPAC Name: dicyclohexyl(2-dicyclohexylphosphanylethyl)phosphane
• InChIKey: BOUYBUIVMHNXQB-UHFFFAOYSA-N
• INCHI: 1S/C26H48P2/c1-5-13-23(14-6-1)27(24-15-7-2-8-16-24)21-22-28(25-17-9-3-10-18-25)26-19-11-4-12-20-26/h23-26H,1-22H2
• Isómeros SMILES: C1CCC(CC1)P(CCP(C2CCCCC2)C3CCCCC3)C4CCCCC4
• WGK Alemania: 3
• Peso molecular: 422.61
• Reaxy-Rn: 960285
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=960285&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organophosphorus compounds
    • Clase Organic phosphines and derivatives

• Kingdom: Organic compounds
• Superclass: Organophosphorus compounds
• Clase: Organic phosphines and derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic phosphines and derivatives
• Alternative Parents: Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Phosphine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as organic phosphines and derivatives. These are organic compounds containing a phosphine derivative, with the general formula B1P(R2)R3 (R1-R3=alkyl, aryl).
• 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

Objetivos asociados (no humanos)

Mus musculus (284745 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

B16 (5829 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive； Air sensitive
• Punto de inflamación (°F): >230 °F
• Punto de inflamación (°C): >110 °C
• Punto de fusión (°C): 92.5-96.5°C
• Peso molecular: 422.600 g/mol
• XLogP3: 6.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 7
• Exact Mass: 422.323 Da
• Monoisotopic Mass: 422.323 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 28
• Formal Charge: 0
• Complexity: 336.000
• 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

Referencias

1. Wen-Jing Pan, Zhong-Xia Wang.  (2018)  Palladium-Catalyzed C−H Benzylation of (Benzo)oxazoles with Benzylic Quaternary Ammonium Triflates.  Asian Journal of Organic Chemistry,  7  (8): (1626-1634).  [PMID:] [10.1002/ajoc.201800264]