2-(4-Nitrophenyl)ethanol, 98%
2-(4-Nitrophenyl)ethanol, 98%
2-(4-Nitrophenyl)ethanol, 98%
Thermo Scientific Chemicals

2-(4-Nitrophenyl)ethanol, 98%

CAS: 100-27-6 | C8H9NO3 | 167.164 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
5 g
25 g
Catalog number H54504.14
also known as H54504-14
Price (USD)
181.65
Special offer
Online exclusive
Ends: 30-Jun-2026
213.00
Save 31.35 (15%)
Each
Quantity:
25 g
Request bulk or custom format
Price (USD)
181.65
Special offer
Online exclusive
Ends: 30-Jun-2026
213.00
Save 31.35 (15%)
Each
Chemical Identifiers
CAS100-27-6
IUPAC Name2-(4-nitrophenyl)ethan-1-ol
Molecular FormulaC8H9NO3
InChI KeyIKMXRUOZUUKSON-UHFFFAOYSA-N
SMILESOCCC1=CC=C(C=C1)[N+]([O-])=O
View more
SpecificationsSpecification SheetSpecification Sheet
FormPowder and/or Lumps
Assay from Supplier's CofA≥97.5%
Appearance (Color)Yellow to yellow-orange to brown
It is a phosphate protecting reagent and O6 of deoxyguanosine.

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
It is a phosphate protecting reagent and O6 of deoxyguanosine.

Solubility
Slightly soluble in water.

Notes
Incompatible with oxidizing agents. Keep at room temperature.
RUO – Research Use Only

General References:

  1. Xiaolian Gao, Barbara L.; Gaffney, Susan Hadden.; Roger A. Jones. Transient protection. 2. One-flask synthesis of 6-O-[(4-nitrophenyl)ethyl]-2'-deoxyguanosine nucleosides. Research Article Prev. Article Next Article Table of Contents Transient protection. 2. One-flask synthesis of 6-O-[(4-nitrophenyl)ethyl]-2'-deoxyguanosine nucleosides Xiaolian Gao, Barbara L. Gaffney, Susan Hadden, Roger A. Jones J. Org. Chem, 51 (5),755-758.
  2. Richard Fuchs.; Calvin A. VanderWerf. Direction of Ring Opening in the Reduction of p-Substituted Styrene Oxides with Lithium Borohydride.J. Am. Chem. Soc. 1954, 76 (6),1631-1634.