2-Nitrobenzyl alcohol, 97%, Thermo Scientific Chemicals
2-Nitrobenzyl alcohol, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-Nitrobenzyl alcohol, 97%, Thermo Scientific Chemicals

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Quantity:
500 g
25 g
100 g
Catalog number A15496.36
also known as A15496-36
Price (USD)/ Each
630.00
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Quantity:
500 g
Request bulk or custom format
Price (USD)/ Each
630.00
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2-Nitrobenzyl alcohol, 97%, Thermo Scientific Chemicals
Catalog numberA15496.36
Price (USD)/ Each
630.00
-
Add to cart
Chemical Identifiers
CAS612-25-9
IUPAC Name(2-nitrophenyl)methanol
Molecular FormulaC7H7NO3
InChI KeyBWRBVBFLFQKBPT-UHFFFAOYSA-N
SMILESOCC1=CC=CC=C1[N+]([O-])=O
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SpecificationsSpecification SheetSpecification Sheet
Melting Point (clear melt)67.0-77.0?C
Appearance (Color)Pale cream to cream
FormPowder
Assay (GC)≥96.0%
The o-nitrobenzyl group (o-NB) is utilized frequently in polymer and materials science. It covers the use of based cross-linkers for photodegradable hydrogels, o-NB side chain functionalization in (block) copolymers, o-NB side chain functionalization for thin film patterning, o-NB for self-assembled monolayers, photo cleavable block copolymers, and photo cleavable bioconjugates.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
The o-nitrobenzyl group (o-NB) is utilized frequently in polymer and materials science. It covers the use of based cross-linkers for photodegradable hydrogels, o-NB side chain functionalization in (block) copolymers, o-NB side chain functionalization for thin film patterning, o-NB for self-assembled monolayers, photo cleavable block copolymers, and photo cleavable bioconjugates.

Solubility
Soluble in water 5000 mg/L 20 deg Celsius.

Notes
Store in cool, dry conditions in a well sealed container. Store away from oxidizing agents.
RUO – Research Use Only

General References:

  1. Hui Zhao; Elizabeth S. Sterner; E. Bryan Coughlin and Patrick Theato. o-Nitrobenzyl Alcohol Derivatives: Opportunities in Polymer and Materials Science. Macromolecules. 2012, 45 (4), 1723-1736.
  2. Aurélien Blanc and Christian G. Bochet. Isotope Effects in Photochemistry. 1. o-Nitrobenzyl Alcohol Derivatives. J. Am. Chem. Soc. 2004, 126 (23), 7174-7175.
  3. Photosensitive protecting reagent for alcohols, acids, phenols etc., cf 4,5-Dimethoxy-2-nitrobenzyl alcohol, L00719. Bis(2-nitrobenzyl) acetals of carbonyl compounds, prepared by acetalization in the presence of 2,2-dimethoxypropane, are cleaved photochemically: J. Chem. Soc., Chem. Commun., 1828 (1985). For reviews of photoremovable groups in organic synthesis, see: Synthesis, 1 (1980); Org. Photochem., 9, 225 (1987).