R-2,2'-dihydroxy-[1,1'-Binaphthalene]-3-carboxaldehyde

98%

  • Product Code: 70291
  CAS:    349149-08-2
Molecular Weight: 314.33406 g./mol Molecular Formula: C₂₁H₁₄O₃
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand or catalyst in organic reactions. Its unique structure allows it to induce chirality in products, making it valuable in the production of enantiomerically pure compounds. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. Additionally, it finds applications in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where high enantiomeric purity is crucial. Its role in facilitating efficient and selective reactions makes it a key component in advanced synthetic chemistry.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.010 10-20 days €127.27
+
-
0.050 10-20 days €505.74
+
-
R-2,2'-dihydroxy-[1,1'-Binaphthalene]-3-carboxaldehyde
This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand or catalyst in organic reactions. Its unique structure allows it to induce chirality in products, making it valuable in the production of enantiomerically pure compounds. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. Additionally, it finds applications in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where high enantiomeric purity is crucial. Its role in facilitating efficient and selective reactions makes it a key component in advanced synthetic chemistry.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Cart

No products

Subtotal: €0.00
€0.00 Total :