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Thermo Scientific Chemicals
2,4-Dichlorobenzoic acid, 98%
CAS: 50-84-0 | C7H4Cl2O2 | 191.007 g/mol
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Catalog number A12372.0B
also known as A12372-0B
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Quantity:
1000 g
Price (USD)
110.65
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123.00Save 12.35 (10%)
Each
Chemical Identifiers
CAS50-84-0
IUPAC Name2,4-dichlorobenzoic acid
Molecular FormulaC7H4Cl2O2
InChI KeyATCRIUVQKHMXSH-UHFFFAOYSA-N
SMILESOC(=O)C1=CC=C(Cl)C=C1Cl
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Specifications
Specification Sheet
Specification SheetAssay (Aqueous acid-base Titration)≥97.5 to ≤102.5%
FormPowder or lumps
Assay (Silylated GC)≥97.5%
Melting Point (clear melt)160.0-166.0?C
Appearance (Color)White
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2,4-Dichlorobenzoic acid is used as reagent during the synthesis of pyrimido[2?,1?:2,3]thiazolo[4,5-b]quinoxaline derivatives. It is also used as starting reagent during the synthesis of 1-(substituted)-1,4-dihydro-6-nitro-4-oxo-7-(sub-secondary amino)-quinoline-3-carboxylic acids.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2,4-Dichlorobenzoic acid is used as reagent during the synthesis of pyrimido[2′,1′:2,3]thiazolo[4,5-b]quinoxaline derivatives. It is also used as starting reagent during the synthesis of 1-(substituted)-1,4-dihydro-6-nitro-4-oxo-7-(sub-secondary amino)-quinoline-3-carboxylic acids.
Solubility
Soluble in ethanol (100 mg/ml), water (0.48 mg/ml), alcohol, ether, and acetone.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
2,4-Dichlorobenzoic acid is used as reagent during the synthesis of pyrimido[2′,1′:2,3]thiazolo[4,5-b]quinoxaline derivatives. It is also used as starting reagent during the synthesis of 1-(substituted)-1,4-dihydro-6-nitro-4-oxo-7-(sub-secondary amino)-quinoline-3-carboxylic acids.
Solubility
Soluble in ethanol (100 mg/ml), water (0.48 mg/ml), alcohol, ether, and acetone.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- A.A. Abu-Hashem.; M.A. Gouda.; F.A. Badria.; A.A. Abu-Hashem.; M.A. Gouda.; F.A. Badria. Synthesis of some new pyrimido[2',1':2,3]thiazolo[4,5-b]quinoxaline derivatives as anti-inflammatory and analgesic agents. European Journal of Medicinal Chemistry. 2010, 45 (5), 1976-1981.
- Palaniappan Senthilkumar.; Murugesan Dinakaran.; Perumal Yogeeswari.; Dharmarajan Sriram.; Arnab China.; Valakunja Nagaraja. Synthesis and antimycobacterial activities of novel 6-nitroquinolone-3-carboxylic acids. European Journal of Medicinal Chemistry. 2009, 44 (1), 345-358.