412600
4-tert-Butyl-2-nitrophenol
97%
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About This Item
Linear Formula:
(CH3)3CC6H3(NO2)OH
CAS Number:
Molecular Weight:
195.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
97%
bp
97 °C/1 mmHg (lit.)
mp
27-29 °C (lit.)
density
1.12 g/mL at 25 °C (lit.)
functional group
nitro
SMILES string
CC(C)(C)c1ccc(O)c(c1)[N+]([O-])=O
InChI
1S/C10H13NO3/c1-10(2,3)7-4-5-9(12)8(6-7)11(13)14/h4-6,12H,1-3H3
InChI key
IHGNADPMUSNTJW-UHFFFAOYSA-N
Application
4-tert-Butyl-2-nitrophenol may be used for the preparation of (2-hydroxy-3-nitro-5-tert-butylbenzyl)trimethylammonium iodide.[1]
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Condensations of N-arylhydroxylamines for the preparation of 5,5'-di-tert-butyl-2,2'-dihydroxydiphenylamine.
Spence JD, et al.
Tetrahedron Letters, 44(4), 849-851 (2003)
Vitaly A Osyanin et al.
The Journal of organic chemistry, 79(3), 1192-1198 (2014-01-15)
The first example of the use of potassium trinitromethanide as a 1,1-ambiphilic synthon equivalent for the construction of a benzofuran moiety mediated by triethylamine has been developed. The method tolerates a variety of functional groups on the starting quaternary ammonium
Yong Zhang et al.
Analytica chimica acta, 899, 75-84 (2015-11-10)
In this research, the applicability of a new sorbent based on boronate affinity material is demonstrated. For this purpose, six strong polar nitrophenols were selected as models which are difficult to be extracted in neutral form (only based on hydrophobic
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