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About This Item
Linear Formula:
(O2N)2C6H3CO2C2H5
CAS Number:
Molecular Weight:
240.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
99%
form
solid
mp
94-95 °C (lit.)
SMILES string
CCOC(=O)c1cc(cc(c1)[N+]([O-])=O)[N+]([O-])=O
InChI
1S/C9H8N2O6/c1-2-17-9(12)6-3-7(10(13)14)5-8(4-6)11(15)16/h3-5H,2H2,1H3
InChI key
IBQREHJPMPCXQA-UHFFFAOYSA-N
General description
Ethyl 3,5-dinitrobenzoate forms charge transfer spectra with n-alkane solutions containing hexakis(n-hexyloxy)triphenylene. Nuclear magnetic resonance spectra of ethyl 3,5-dinitrobenzoate was studied.
Signal Word
Warning
Hazard Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
13 - Non 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)
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The mechanism of action of ethanolamine deaminase. I. Studies with isotopic hydrogen and oxygen.
B M Babior
The Journal of biological chemistry, 244(2), 449-456 (1969-01-25)
Aggregates of hexakis (n-hexyloxy) triphenylene self-assemble in dodecane solution: intercalation of (-)-menthol 3, 5-dinitrobenzoate induces formation of helical structures.
Gallivan JP and Schuster GB.
The Journal of Organic Chemistry, 60(8), 2423-2429 (1995)
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