4-Fluoro-N-methylbenzylamine
Based on 1 Customer Validation
4-Fluoro-N-methylbenzylamine is a secondary amine that can serve as a model substrate for BODIPY photoprotecting group studies. 4-Fluoro-N-methylbenzylamine can react with an activated p-nitrophenyl BODIPY carbonate to give the corresponding carbamate caged adduct; moreover, under 530 nm green-light photolysis conditions, it can be released from the caged carbamate conjugate.
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- CAS No.: 405-66-3
- Formula: C8H10FN
- Molecular Weight:139.17
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Storage:
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Biological Activity
Description
In Vitro
4‑Fluoro‑N‑methylbenzylamine can react with activated BODIPY p‑nitrophenyl carbonate to generate carbamate-caged conjugates 11‑14[1].
4‑Fluoro‑N‑methylbenzylamine can be cleanly released from caged carbamate conjugates under 530 nm green-light photolysis conditions[1].
4‑Fluoro‑N‑methylbenzylamine bears a fluorine substituent, enabling convenient quantitative reaction monitoring by 19F NMR spectroscopy[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. .
Chemical Information
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CAS No. 405-66-3
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Appearance Liquid (Density: 1.056 g/cm3)
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Molecular Weight 139.17
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Formula C8H10FN
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Color Colorless to light yellow
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SMILES
CNCC1=CC=C(C=C1)F
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Purity & Documentation
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Data Sheet (266 KB)
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SDS (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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Handling Instructions (2659 KB)
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)