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BINAP

BINAP structure

BINAP 

structure
  • CAS No:

    98327-87-8

  • Formula:

    C44H32P2

  • Chemical Name:

    BINAP

  • Synonyms:

    Phosphine,1,1′-[1,1′-binaphthalene]-2,2′-diylbis[1,1-diphenyl-;Phosphine,[1,1′-binaphthalene]-2,2′-diylbis[diphenyl-;1,1′-[1,1′-Binaphthalene]-2,2′-diylbis[1,1-diphenylphosphine];BINAP;2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl;rac-BINAP;(±)-BINAP;rac-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl;[1,1′-Binaphthalene]-2,2′-diylbis[diphenylphosphine];2,2′-Bis(diphenylphosphanyl)-1,1′-binaphthyl;2,2′-Bis(diphenylphosphino)-1,1′-binaphthalene;(±)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthalene;1,1′-Binaphthalene-2,2′-diylbis(diphenylphosphane);(±)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl;76144-87-1

  • Categories:

    Organic Chemistry  >  Phosphines

Description

1.1'-Binaphthyl-2.2'-diphemyl phosphine is White to light beige powder


2,2'-Bis(diphenylphosphino)-1,1'-dinaphthalene is a powerful chiral auxiliary that is used as a homogeneous catalyst in some asymmetric chemical syntheses. 2,2'-Bis(diphenylphosphino)-1,1'-dinaphthalene is utilized for its high enantioselectivity and is used as a ligand to create coordination complexes.

BINAP Basic Attributes

622.67

622.67

5321443

1308068-626-2

29319090

Characteristics

0

11.4

White to light beige Powder

230-231 °C (decomp)

724.3°C at 760 mmHg

419.0±37.8 °C

soluble in tetrahydrofuran, benzene and dichloromethane. Slightly soluble in ether, methanol and ethanol. Insoluble in water.

Store in a cool, dry place. Store in a tightly closed container.

Safety Information

NONH for all modes of transport

3

36/37/38

22-24/25-37/39-26

Xi

Stable under normal temperatures and pressures.

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

BINAP Use and Manufacturing

racemic-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl ( (+/-)-BINAP ) is an essential role in the organic synthesis of enantioselective transformations catalyzed by the complexes of ruthenium, rhodium and palladium. It is also employed in palladium-catalyzed arylamine coupling in the preparation of demethylthiocholchines. used with Cu(II) to catalyze the addition of arylsulfonamides to styrenes and olefins.

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