Substance
ID:328145
Names and Identifiers
Synonyms
2,4,6-Trichlorobenzoic acid2,4,6-三氯苯甲酸
IUPAC name
2,4,6-trichlorobenzoic acid
IUPAC Traditional name
2,4,6-trichlorobenzoic acid
Properties
Safety Information
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Safety Statements
26-37/39
German water hazard class
3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
GHS Signal Word
Warning
GHS Precautionary statements
P261-P305+P351+P338
MSDS Link
GHS Hazard statements
H315-H319-H335
Risk Statements
36/37/38
European Hazard Symbols
Irritant (Xi)RTECS
DH8050000
Physical Property
Melting Point
160-164 °C(lit.)
Product Information
Linear Formula
Cl3C6H2CO2H
Molecule Details
Packaging
10 g in poly bottle
Application
Reactant involved in:
• Active-sodium-promoted reductive cleavage of halogenated benzoic acids1
• Synthesis of aryl aminopyrazole benzamides for use as non-steroidal selective glucocorticoid receptor agonists2
• Flame retardant monomer synthesis3
• Synthesis of 3,4,7-trisubstituted coumarins for use as antifungals4
• Solid-phase synthesis of saphenamycin analogs with antimicrobial activity5Cocatalyst for cis-dihydroxylation and epoxidation of alkenes6
10 g in poly bottle
Application
Reactant involved in:
• Active-sodium-promoted reductive cleavage of halogenated benzoic acids1
• Synthesis of aryl aminopyrazole benzamides for use as non-steroidal selective glucocorticoid receptor agonists2
• Flame retardant monomer synthesis3
• Synthesis of 3,4,7-trisubstituted coumarins for use as antifungals4
• Solid-phase synthesis of saphenamycin analogs with antimicrobial activity5Cocatalyst for cis-dihydroxylation and epoxidation of alkenes6
Molecular Spectra
No Data Available
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References
No Data Available
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