CAS 602-09-5

BINOL

Description:

BINOL, or 1,1'-bi-2-naphthol, is a chiral organic compound characterized by its two naphthol units linked by a single bond. It is a colorless to pale yellow crystalline solid that is sparingly soluble in water but soluble in organic solvents such as ethanol and ether. BINOL exhibits strong optical activity due to its chiral nature, making it valuable in asymmetric synthesis and as a chiral ligand in various catalytic processes. The compound has a melting point that typically falls within a specific range, and it can undergo various chemical reactions, including oxidation and esterification. BINOL is also known for its ability to form stable complexes with metal ions, which enhances its utility in catalysis. Its derivatives and modifications are widely studied in the field of organic chemistry, particularly in the development of enantioselective reactions. Overall, BINOL is a significant compound in both academic research and industrial applications due to its unique properties and versatility.

Formula: C₂₀H₁₄O₂

InChI: InChI=1S/C20H14O2/c21-17-11-9-13-5-1-3-7-15(13)19(17)20-16-8-4-2-6-14(16)10-12-18(20)22/h1-12,21-22H

InChI key: InChIKey=PPTXVXKCQZKFBN-UHFFFAOYSA-N

SMILES: OC1=C(C2=C(C=C1)C=CC=C2)C=3C4=C(C=CC3O)C=CC=C4

Synonyms:

• (.+-.)-1,1'-Bi-2-naphthol
• (.+-.)-1,1'-Binaphthyl-2,2'-diol
• (.+-.)-2,2'-Dihydroxy-1,1'-binaphthalene
• (.+-.)-2,2'-Dihydroxy-1,1'-binaphthyl
• (.+-.)-2,2'-Dihydroxy-1,1'-dinaphthyl
• (.+-.)-Bi-β-naphthol
• (.+-.)-Binol
• (RS)-1,1'-Bi-2,2'-naphthol
• (RS)-1,1'-Bi-2-naphthol
• 1,1'-Bi(β-naphthol)
• 1,1'-Binaftilo-2,2'-Diol
• 1,1'-Binaphtyle-2,2'-diol
• 1,1'-Bis-2-naphthol
• 1-(2-Hydroxynaphthalen-1-yl)naphthalen-2-ol
• 2,2'-Dihydroxybinaphthalene
• 2,2'-Dihydroxydinaphthyl
• 2,2'-Dinaphthol
• Bis-β-naphthol
• Nsc 27049
• Rac-2,2′-dihydroxy-1,1′-binaphthyl
• Racemic 2,2'-dihydroxy-1,1'-binaphthyl
• α-Binaphthyl-2,2'-diol
• β-Binaphthol
• [1,1′-Binaphthalene]-2,2′-diol
• 1,1'-Bi-naphthol

(+/-)-1,1'-Bi(2-naphthol), 99%

CAS: 602-09-5

()-1,1'-Bi(2-naphthol) acts as chiral separation agents. It is widely used in chiral liquid crystal,medicines,spices etc,. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. T

Formula: C₂₀H₁₄O₂

Purity: 99%

Color and Shape: Powder, White to pale cream to pale brown

Molecular weight: 286.33

Ref: 02-A11182

racemic-1,1'-Bi-2-naphthol, 99% rac-BINOL

CAS: 602-09-5

racemic-1,1'-Bi-2-naphthol, 99% rac-BINOL

Formula: C₂₀H₁₄O₂

Purity: 99%

Color and Shape: white pwdr.

Molecular weight: 286.32

Ref: 08-08-0999

2,2′-Dihydroxy-1,1′-dinaphthyl

CAS: 602-09-5

Formula: C₂₀H₁₄O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 286.33

Ref: 10-F003403

[1,1'-Binaphthalene]-2,2'-diol

CAS: 602-09-5

Formula: C₂₀H₁₄O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 286.3240

Ref: IN-DA00IKFQ

1,1''-Bi-2-naphthol

CAS: 602-09-5

Formula: C₂₀H₁₄O₂

Molecular weight: 286.33

Ref: 7W-GK5275

2,2'-Dihydroxy-[1,1']-binaphthyl

CAS: 602-09-5

2,2'-Dihydroxy-[1,1']-binaphthyl

Purity: 99%

Molecular weight: 286.32g/mol

Ref: 54-OR30345

1,1'-Bi-2-naphthol

CAS: 602-09-5

Formula: C₂₀H₁₄O₂

Purity: >99.0%(GC)

Color and Shape: White to Gray to Brown powder to crystal

Molecular weight: 286.33

Ref: 3B-B0461

2,2'-Dihydroxy-1,1'-dinaphthyl

CAS: 602-09-5

2,2'-Dihydroxy-1,1'-dinaphthyl (DHDP) is a chiral molecule that has been used in analytical chemistry to determine the enantiomeric purity of alkanoic acid and fatty acids. The molecule exhibits intramolecular hydrogen bonding interactions with the hydroxyl group on one side and the asymmetric carbon atom on the opposite side. DHDP can also form hydrogen bonds with amines and sodium salts. The x-ray crystal structures of DHDP reveal magnesium ions bound to the N atom, which stabilizes the molecule by forming intermolecular hydrogen bonds.

Formula: C₂₀H₁₄O₂

Purity: Min. 99 Area-%

Molecular weight: 286.33 g/mol

Ref: 3D-FD07749