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Sigma-Aldrich

3,5-Dinitrobenzyl alcohol

98%

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About This Item

Linear Formula:
(O2N)2C6H3CH2OH
CAS Number:
71022-43-0
Molecular Weight:
198.13
Beilstein:
2054388
EC Number:
275-131-1
MDL number:
MFCD00007235
UNSPSC Code:
12352100
PubChem Substance ID:
24851094
NACRES:
NA.22

Quality Level

100

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
Ludmila Eisner et al.
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A sensor for trinitrotoluene (TNT) detection was developed by using a combination of optical micro-ring technology and a receptor coating based on molecularly imprinted sol-gel layers. Two techniques for deposition of receptor layers were compared: Airbrush technology and electrospray ionization.
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
Evon Powell et al.
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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