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(S)-BINOL - ≥99% , CAS No.18531-99-2

En stock
SKU
B100620
Articles du produit groupé
Nom du produit Qté
[B100620-1g] (S)-BINOL (1g)
9,90 $US
[B100620-5g] (S)-BINOL (5g)
11,90 $US
[B100620-25g] (S)-BINOL (25g)
21,90 $US
[B100620-100g] (S)-BINOL (100g)
75,90 $US
[B100620-500g] (S)-BINOL (500g)
337,90 $US

(S)-BINOL ligand in combination with titanium(IV) isopropoxide, forms (S)-(-)-BINOL-Ti complex, which is an effective chiral catalyst for: ? asymmetric addition of alkynylzinc to unactivated ketones ? enantioselective ring-opening reaction of meso-stilbene oxide and cyclohexene oxide with anilines ? asymmetric aryl transfers from triaryl(tetrahydrofuran)aluminum reagents to a wide variety of ketones It can also react with zirconium(IV) isopropoxide isopropanol complex to form a chiral Lewis acid catalyst for the facile enantioselective allylation of aldehydes by allyltributyltin. Precursor to phosphoramidite catalyst employed in a conversion of allylic alcohols to allylic amines.

Plus d’information

Plus d’information
CAS18531-99-2
Synonymes(S)-BINOL | (+/-)-1,1'-Binaphthalene-2,2'-diol | 1-(2-hydroxy-1-naphthalenyl)-2-naphthalenol | (1r)-[1,1'-binaphthalene]-2,2'-diol | (S)-(-)-1,1'-Bi(2-naphthol) | [1,1']Binaphthalenyl-2,2'-diol | AI3-19388 | Binol (R)-(+)-form [MI] | (R)-(+)-1,1'-Bi(2-nap
Spécifications et pureté≥99%
Conditions de stockage de stockageStore at 2-8°C
Expédié enWet ice
Product Description

(S)-BINOL ligand in combination with titanium(IV) isopropoxide, forms (S)-(-)-BINOL-Ti complex, which is an effective chiral catalyst for: ? asymmetric addition of alkynylzinc to unactivated ketones ? enantioselective ring-opening reaction of meso-stilbene oxide and cyclohexene oxide with anilines ? asymmetric aryl transfers from triaryl(tetrahydrofuran)aluminum reagents to a wide variety of ketones It can also react with zirconium(IV) isopropoxide isopropanol complex to form a chiral Lewis acid catalyst for the facile enantioselective allylation of aldehydes by allyltributyltin. Precursor to phosphoramidite catalyst employed in a conversion of allylic alcohols to allylic amines.

Pubchem Sid508811088
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/508811088
SolubilitéInsoluble in water; Soluble in Ethanol,Tetrahydrofuran; Slightly soluble in Toluene
Numéro MdlMFCD00004068
Numéro CE606-050-5
PubChem CID11762
Formule moléculaireC20H14O2

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