Manufacturer Supply with High Purity and Stable Quality
(1R,2S)-(-)-2-Amino-1,2-Diphenylethanol CAS: 23190-16-1
(1S,2R)-(+)-2-Amino-1,2-Diphenylethanol CAS: 23364-44-5
| Chemical Name | (1S,2R)-(+)-2-Amino-1,2-Diphenylethanol |
| CAS Number | 23364-44-5 |
| CAT Number | RF-CC167 |
| Stock Status | In Stock, Production Scale Up to Tons |
| Molecular Formula | C14H15NO |
| Molecular Weight | 213.28 |
| Brand | Ruifu Chemical |
| Item | Specifications |
| Appearance | White or Off-White Crystallized Powder |
| Specific Rotation | +6.0° ~ +8.0° (C=0.6, EtOH) |
| Clarity | Clear |
| Melting Point | 141.0~144.0℃ |
| Water | ≤0.50% |
| e.e | ≥99.0% |
| Assay | ≥99.0% |
| Test Standard | Enterprise Standard |
| Usage | Chiral Compounds; Pharmaceutical Intermediates |
Package: Bottle, Aluminum 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.
Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of (1S,2R)-(+)-2-Amino-1,2-Diphenylethanol (CAS: 23364-44-5) with high quality.
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.
Ligand used to make chiral oxaborolidines for the enantioselective alkynylation of aldehydes
Ligand used in organoindium reagents for asymmetric Barbier-type allylations
Ligand used in organoindium reagents for asymmetric Barbier-type propargylations
Application
(1S,2R)-(+)-2-Amino-1,2-diphenylethanol can be used:
To prepare vanadium(V) Schiff base complexes, which are used as catalysts in the oxidation of sulfides and olefins.
To prepare chiral selectors, which are immobilized on aminated silica gel, applicable as chiral stationary phase in HPLC.
To immobilize on the frame of α-zirconium phosphate to yield layered zirconium phosphonates, which are used in the heterogeneous catalysis.
As a chiral auxiliary in the preparation of homopropargylic alcohols from aliphatic and aromatic aldehydes.