All Photos(4)
About This Item
Linear Formula:
(O2N)2C6H3CH2OH
CAS Number:
Molecular Weight:
198.13
Beilstein/REAXYS Number:
2054388
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
98%
mp
88-91 °C (lit.)
SMILES string
OCc1cc(cc(c1)[N+]([O-])=O)[N+]([O-])=O
InChI
1S/C7H6N2O5/c10-4-5-1-6(8(11)12)3-7(2-5)9(13)14/h1-3,10H,4H2
InChI key
GPHYIQCSMDYRGJ-UHFFFAOYSA-N
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General description
3,5-Dinitrobenzyl alcohol on reaction with p-toluenesulphonyl chloride yields 3,5-dinitrobenzyl p-toluenesulphonate.
Application
3,5-Dinitrobenzyl alcohol was used in the synthesis of 3,5-bis((bezoxycarbonyl)imino)benzyl alcohol.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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K Funazo et al.
Journal of chromatography, 481, 211-219 (1989-11-03)
New UV-labelling agents have been synthesized, which are designed to convert monocarboxylic acids into their highly UV-absorbing derivatives for enhancement of the sensitivities of UV detection in high-performance liquid chromatography. The reagents are p-nitrobenzyl, 3,5-dinitrobenzyl and 2-(phthalimino)ethyl p-toluenesulphonates. Each has
Synthesis and characterization of hyperbranched polyurethanes prepared from blocked isocyanate monomers by step-growth polymerization.
Spindler R and Frechet JMJ.
Macromolecules, 26(18), 4809-4813 (1993)
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International journal of nanomedicine, 2(3), 449-459 (2007-11-21)
The interaction of the important but often overdosed local anesthetic bupivacaine, its structural analogs 2,6-dimethylaniline, and N-methyl-2,6-dimethylacetanilide, and cocaine, with several electron deficient aromatic moieties were studied primarily by proton NMR and UV-visible spectroscopy. In solution, the anesthetic, its analogs
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