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Excellent quality Dimethyl D-(-)-Tartrate - (1S,2R)-(+)-2-Amino-1,2-Diphenylethanol CAS 23364-44-5 e.e ≥99.0% Assay ≥99.0% High Purity – Ruifu

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.