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CAS RN: 57583-53-6 | Product Number: D4413
N,N'-Dihydroxypyromellitimide
Purity: >96.0%(HPLC)(N)
Synonyms:
- N,N'-Dihydroxypyromellitic Diimide
- NDHPI
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days |
---|---|---|---|
1G |
$140.00
|
≥40 | ≥100 |
5G |
$427.00
|
4 | 8 |
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Product Number | D4413 |
Purity / Analysis Method | >96.0%(HPLC)(N) |
Molecular Formula / Molecular Weight | C__1__0H__4N__2O__6 = 248.15 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image) |
CAS RN | 57583-53-6 |
Reaxys Registry Number | 9640376 |
PubChem Substance ID | 253661830 |
Specifications
Appearance | White to Light yellow powder to crystal |
Purity(HPLC) | min. 96.0 area% |
Purity(with Total Nitrogen) | min. 96.0 % |
Properties (reference)
Solubility (slightly sol. in) | Dimethylformamide |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
Precautionary Statements | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
Related Laws:
Transport Information:
H.S.code* | 2928.00-000 |
Application
Metal-Free Fluorination of C(sp3)-H Bonds using a Catalytic N-Oxyl Radical
Typical Procedure: To a solution of 4-phenylbutyl benzoate (55.6 mg, 0.219 mmol) and NDHPI (1.36 mg, 0.00547 mmol) in MeCN (2.2 mL) is added F-TEDA-BF4 (155 mg, 0.438 mmol) at room temperature. The mixture is degassed by freeze-thaw for 3 times under Ar atmosphere, and stirred at 50 °C for 5 h. The reaction mixture is then neutralized with saturated aqueous NaHCO3, and extracted with EtOAc (3 mL×3). The combined organic layers are dried over Na2SO4, and concentrated. The residue is purified with flash column chromatography (silica gel, hexane : Et2O=30 : 1) to provide 4-benzoyloxy-1-phenylbutyl fluoride (43.1 mg, Y. 72%).
References
- Metal-free fluorination of C(sp3)-H bonds using a catalytic N-oxyl radical
PubMed Literature
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