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184144

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

Assay

98%

mp

88-91 °C (lit.)

functional group

hydroxyl
nitro

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCR4990
MKCR9722
SHBL8281
SHBG1648V
67396TJV

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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.
Sensors (Basel, Switzerland), 19(18) (2019-09-13)
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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