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CAS RN: 2973-59-3 | Product Number: B4681
2-Bromo-5-hydroxy-4-methoxybenzaldehyde
Purity: >97.0%(GC)(T)
Synonyms:
- 6-Bromoisovanillin
Product Documents:
Size | Unit Price | Belgium | Japan* | Quantity |
---|---|---|---|---|
5G |
436,00 €
|
1 | 20 |
|
*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 | B4681 |
Purity / Analysis Method | >97.0%(GC)(T) |
Molecular Formula / Molecular Weight | C__8H__7BrO__3 = 231.05 |
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 |
CAS RN | 2973-59-3 |
Reaxys Registry Number | 1942858 |
PubChem Substance ID | 468590523 |
MDL Number | MFCD00195552 |
Specifications
Appearance | White to Light yellow powder to crystal |
Purity(GC) | min. 97.0 % |
Purity(Neutralization titration) | min. 97.0 % |
NMR | confirm to structure |
Properties (reference)
Melting Point | 116 °C |
Boiling Point | 280 °C |
Solubility (soluble in) | Methanol |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H317 : May cause an allergic skin reaction. H411 : Toxic to aquatic life with long lasting effects. |
Precautionary Statements | P261 : Avoid breathing dust. P273 : Avoid release to the environment. P280 : Wear protective gloves. P391 : Collect spillage. P362 + P364 : Take off contaminated clothing and wash it before reuse. P333 + P313 : If skin irritation or rash occurs: Get medical advice/ attention. |
Related Laws:
Transport Information:
UN Number | UN3077 |
Class | 9 |
Packing Group | III |
HS Number | 2913000090 |
Application
A Synthetic Intermediate of Galanthamine
This product is used for the synthesis galanthamine which is an acetylcholinesterase (AChE) inhibitor.
References
- New kilogram-synthesis of the Anti-Alzheimer drug (-)-galanthamine
- Development of a pilot scale process for the anti-Alzheimer drug (-)-galanthamine using large-scale phenolic oxidative coupling and crystallisation-induced chiral conversion
Product Documents (Note: Some products will not have analytical charts available.)
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