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About This Item
Linear Formula:
(O2N)2C6H2(CH3)CO2H
CAS Number:
Molecular Weight:
226.14
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
mp
205-207 °C (lit.)
functional group
carboxylic acid
SMILES string
Cc1c(cc(cc1[N+]([O-])=O)[N+]([O-])=O)C(O)=O
InChI
1S/C8H6N2O6/c1-4-6(8(11)12)2-5(9(13)14)3-7(4)10(15)16/h2-3H,1H3,(H,11,12)
InChI key
CDVNZMKTJIBBBV-UHFFFAOYSA-N
General description
Synthesis of a series of heterocyclic derivatives of 3,5-dinitro-o-toluic acid has been reported.
Application
3,5-Dinitro-o-toluic acid was used in the synthesis of isoquinolone.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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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Find documentation for the products that you have recently purchased in the Document Library.
Pyridine annelation of o-methyl arylcarboxylic acids with vilsmeier reagents.
Meth-Cohn O and Taljaard HC.
Tetrahedron Letters, 24(42), 4607-4610 (1983)
Synthesis of some heterocyclic derivatives of 3, 5-dinitro o-toluic acid.
Wu MT.
Journal of Heterocyclic Chemistry, 9, 31-31 (1972)
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