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CAS RN: 214754-50-4 | Product Number: M3572
2-Hydroxy-5-methoxyisoindoline-1,3-dione
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Purity: >98.0%(T)(HPLC)
Synonyms:
- 4-Methoxy-N-hydroxyphthalimide
- 2-Hydroxy-5-methoxy-1H-isoindole-1,3(2H)-dione
Product Documents:
| Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time |
Shipping Information
|
|---|---|---|---|---|---|
| 1G |
$45.00
|
12 | 0 | Contact Us | |
| 5G |
$172.00
|
2 | 0 | Contact Us |
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* The storage conditions are subject to change without notice.
| Product Number | M3572 |
| Purity / Analysis Method | >98.0%(T)(HPLC) |
| Molecular Formula / Molecular Weight | C__9H__7NO__4 = 193.16 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Air Sensitive |
| Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image) |
| CAS RN | 214754-50-4 |
| Reaxys Registry Number | 8765278 |
Specifications
| Appearance | White to Light yellow powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Purity(Neutralization titration) | min. 98.0 % |
| Melting point | 218.0 to 222.0 °C |
| NMR | confirm to structure |
Properties (reference)
| Melting Point | 220 °C |
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
N-Hydroxyphthalimide Derivatives for the Synthesis of Redox Active Esters
References
- 1) Control of Redox-Active Ester Reactivity Enables a General Cross-Electrophile Approach to Access Arylated Strained Rings
- 2) Nickel-Catalyzed C(sp3)–C(sp3) Cross-Electrophile Coupling of In Situ Generated NHP Esters with Unactivated Alkyl Bromides
Articles/Brochures
TCIMAIL
[Product Highlights] N-Hydroxyphthalimide Derivatives for the Synthesis of Redox Active EstersProduct Documents (Note: Some products will not have analytical charts available.)
Safety Data Sheet (SDS)
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Specifications
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