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CAS RN: 70627-52-0 | Product Number: B4301
4'-(Benzyloxy)benzylidene-4-fluoroaniline
![4'-(Benzyloxy)benzylidene-4-fluoroaniline No-Image](/medias/B4301.jpg?context=bWFzdGVyfHJvb3R8NTY1MjR8aW1hZ2UvanBlZ3xhR0UyTDJoaVlpODRPVEl3TWpZeU9UWTNNekkyTDBJME16QXhMbXB3Wnd8MzM5ZmZjNjUzODE5OTJjYWNmYzY4MDdjNTc0NmI0YWVmN2MxODVmNzdkNWUxOGJiM2ZkMDdiYzFjMmMwY2RkOQ)
Purity: >98.0%(GC)
Synonyms:
Product Documents:
Size | Unit Price | Belgium | Japan* | Quantity |
---|---|---|---|---|
5G |
€45.00
|
1 | 2 |
|
25G |
€175.00
|
1 | 7 |
|
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
Product Number | B4301 |
Purity / Analysis Method | >98.0%(GC) |
Molecular Formula / Molecular Weight | C__2__0H__1__6FNO = 305.35 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
CAS RN | 70627-52-0 |
Reaxys Registry Number | 8420758 |
PubChem Substance ID | 253659912 |
MDL Number | MFCD00017951 |
Specifications
Appearance | White to Light yellow powder to crystal |
Purity(GC) | min. 98.0 % |
Melting point | 134.0 to 138.0 °C |
NMR | confirm to structure |
Properties (reference)
Melting Point | 136 °C |
Solubility (soluble in) | Toluene |
GHS
Related Laws:
Transport Information:
HS Number | 2921420090 |
Application
Synthesis of Azetidinone-Based Cholesterol Absorption Inhibitors
B4301 is used for the synthesis of azetidinone-based cholesterol absorption inhibitors.
References
- Discovery of 1-(4-Fluorophenyl)-(3R)-[3-(4-fluorophenyl)-(3S)-hydroxypropyl]-(4S)-(4-hydroxyphenyl)-2-azetidinone (SCH 58235): A Designed, Potent, Orally Active Inhibitor of Cholesterol Absorption
- A Novel One-Step Diastereo- and Enantioselective Formation of trans-Azetidinones and Its Application to the Total Synthesis of Cholesterol Absorption Inhibitors
- Synthesis of 3-arylpropenyl, 3-arylpropynyl and 3-arylpropyl 2-azetidinones as cholesterol absorption inhibitors: application of the palladium-catalyzed arylation of alkenes and alkynes
- Formal asymmetric synthesis of a cholesterol absorption inhibitor bearing a 2-azaspiro[3.5]nonan-1-one moiety
- Heterocyclic ring scaffolds as small-molecule cholesterol absorption inhibitors
PubMed Literature
Product Documents (Note: Some products will not have analytical charts available.)
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