(R)-(+)-1,1′-Bi-2-naphthol CAS 18531-94-7 Assay ≥99.5% (HPLC) e.e≥99.5% High Purity

Short Description:

Chemical Name: (R)-(+)-1,1′-Bi-2-naphthol

Synonyms: (R)-(+)-BINOL

CAS: 18531-94-7

Appearance: White Crystalline Powder

Chiral Assay: e.e ≥99.5% (HPLC) Chiral Column

Chemical Assay: ≥99.5% (HPLC)

Chiral Compounds, High Quality, Commercial Production


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Description:

Chemical Properties:

Chemical Name (R)-(+)-1,1'-Bi-2-naphthol
Synonyms (R)-(+)-BINOL
CAS Number 18531-94-7
CAT Number RF-CC216
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C20H14O2
Molecular Weight 286.32
Density 1.301
Brand Ruifu Chemical

Specifications:

Item Specifications
Appearance White Crystalline Powder
Loss on Drying ≤0.50%
Melting Point 208.0~210.0℃
Specific Rotation [a]22/D +34.0° ~ +37.0° (C=1 in THF)
Chiral Assay  e.e ≥99.5% (HPLC) Chiral Column
Chemical Assay ≥99.5% (HPLC) 
Test Standard Enterprise Standard
Usage Chiral Compounds; Pharmaceutical Intermediates 

Package & Storage:

Package: Bottle, Aluminium foil bag, Cardboard Drum, 25kg/Drum, or according to customer's requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.

Advantages:

1

FAQ:

Application:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of (R)-(+)-1,1'-Bi-2-naphthol (CAS: 18531-94-7) with high quality, widely used in organic synthesis, synthesis of pharmaceutical intermediates and fine chemical synthesis.

Shanghai Ruifu Chemical Co., Ltd. plays an important role in the chiral chemistry, the company is committed to the production of chiral compounds. Our products are widely praised by customers.

(R)-(+)-1,1'-Bi-2-naphthol (CAS: 18531-94-7) is obtained through resolution of racemic BINOL, which is usually made from 2-naphthol catalyzed by iron(III) chloride through radical reaction. (R)-(+)-1,1'-Bi-2-naphthol has been widely used for various applications: 1) chiral inducing agents for catalytic, asymmetric reactions such as the Diels-Alder reaction,ene reaction,or as Lewisacids; 2) enantioselective reduction of ketones; 3) synthesis of chiral macrocyclesand otherinteresting compounds. A chiral binapthol imminium salt precursor used in the catalytic asymmetric oxidation of sulfides to sulfoxides. Chiral lanthanide triflates formed from binaphthol serve as catalysts for asymmetric Diels-Alder reactions. Derivatives of binaphthol have recently been used in asymmetric Claisen rearrangements and asymmetric epoxidations. The lithium aluminum hydride derivative of these diols (BINAP-H) has been used extensively for the reduction of ketones. It is used in biosynthetic preparation for enantioselective oxidation of naphthols to binaphthyldiols with horseradish peroxidase catalyst.

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