Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
(O2N)2C6H3CH2OH
CAS Number:
Molecular Weight:
198.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
275-131-1
Beilstein/REAXYS Number:
2054388
MDL number:
Product Name
3,5-Dinitrobenzyl alcohol, 98%
InChI key
GPHYIQCSMDYRGJ-UHFFFAOYSA-N
InChI
1S/C7H6N2O5/c10-4-5-1-6(8(11)12)3-7(2-5)9(13)14/h1-3,10H,4H2
SMILES string
OCc1cc(cc(c1)[N+]([O-])=O)[N+]([O-])=O
assay
98%
mp
88-91 °C (lit.)
functional group
hydroxyl
nitro
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
3,5-Dinitrobenzyl alcohol was used in the synthesis of 3,5-bis((bezoxycarbonyl)imino)benzyl alcohol.
General description
3,5-Dinitrobenzyl alcohol on reaction with p-toluenesulphonyl chloride yields 3,5-dinitrobenzyl p-toluenesulphonate.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service