Chemical Properties:
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.Commercial Supply Dapoxetine Hydrochloride and Related Intermediates: 3-Chloropropiophenone CAS: 936-59-4 (S)-3-Amino-3-Phenylpropan-1-ol CAS: 82769-76-4 (S)-3-Amino-3-Phenylpropanoic Acid CAS: 40856-44-8 (R)-Diphenylprolinol CAS: 22348-32-9 (S)-Diphenylprolinol CAS: 112068-01-6 (S)-(-)-3-Chloro-1-Phenyl-1-Propanol CAS: 100306-34-1 Dapoxetine Hydrochloride CAS: 129938-20-1| Item | Specifications |
| Appearance | White Crystals |
| Identification | IR, HPLC |
| Melting Point | 77.0~80.0℃ |
| Purity (HPLC) | ≥99.0% |
| E.E (HPLC) | ≥99.0% e.e |
| Specific Rotation [α]D20 | -64.0°~-70.0° (C=3, Methanol 25℃) |
| Moisture (K.F) | <0.10% |
| Single Impurity | ≤0.50% |
| Total Impurities | ≤1.0% |
| Test Standard | Enterprise Standard |
| Usage | Chiral Compounds; Pharmaceutical Intermediates |
Description:
Specifications:
Package & Storage:
| Chemical Name | (S)-Diphenylprolinol |
| Synonyms | (S)-(-)-α,α-Diphenyl-2-Pyrrolidinemethanol;(S)-(-)-ɑ,ɑ-Diphenylprolinol; (S)-2-(Hydroxydiphenylmethyl)pyrrolidine; (S)-1,1-Diphenylprolinol; (S)-(-)-2-(Diphenylhydroxymethyl)pyrrolidine |
| CAS Number | 112068-01-6 |
| CAT Number | RF-CC115 |
| Stock Status | In Stock, Production Scale Up to Tons |
| Molecular Formula | C17H19NO |
| Molecular Weight | 253.34 |
| Solubility | Soluble in Chloroform |
| Shipping Condition | Shipped Under Ambient Temperature |
| Brand | Ruifu Chemical |
Advantages:
FAQ:
Application:
Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of (S)-Diphenylprolinol (CAS: 112068-01-6) with high quality, used in synthesis of active pharmaceutical ingredient (API). (S)-Diphenylprolinol (CAS: 112068-01-6) is a kind of alcohols, which can be used as pharmaceutical intermediates. (S)-Diphenylprolinol is a compound used to prepare the corresponding oxazaborolidines for the borane-mediated asymmetric reduction of ketones.
