Substance
ID:340667
Names and Identifiers
IUPAC Traditional name
chloranil
Synonyms
p-Chloranil2,3,5,6-四氯-1,4-苯醌Tetrachloro-1,4-benzoquinone四氯对醌2,3,5,6-Tetrachloro-1,4-benzoquinone四氯苯醌四氯-1,4-苯醌Chloranil
IUPAC name
tetrachlorocyclohexa-2,5-diene-1,4-dione
Registration numbers
CAS Number
EC Number
MDL Number
Beilstein Number
PubChem SID
Properties
Safety Information
European Hazard Symbols
Nature polluting (N)
Irritant (Xi)GHS Precautionary statements
P273-P305+P351+P338-P501
Risk Statements
36/38-50/53
UN Number
3077
MSDS Link
GHS Pictograms
Hazardous to the aquatic environment
Acute hazard, category1
Chronic hazard, categories 1,2
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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Packing Group
3
RID/ADR
UN 3077 9/PG 3
GHS Signal Word
Warning
RTECS
DK6825000
GHS Hazard statements
H315-H319-H410
Safety Statements
37-60-61
Hazard Class
9
German water hazard class
2
Pharmacology Properties
Gene Information
human ... ACHE(43), BCHE(590), CES1(1066)
Physical Property
Melting Point
289 °C (dec.)(lit.)
Product Information
Purity
99%
Linear Formula
C6Cl4(=O)2
Molecule Details
Packaging
25, 100 g in poly bottle
Application
Synthesis of dibenzofurans via oxidative cyclization.1
Undergoes photoinduced cycloaddition reactions with stilbene derivatives and α,β-unsaturated carbonyl compounds. Fluorescence quencher.
25, 100 g in poly bottle
Application
Synthesis of dibenzofurans via oxidative cyclization.1
Undergoes photoinduced cycloaddition reactions with stilbene derivatives and α,β-unsaturated carbonyl compounds. Fluorescence quencher.
Molecular Spectra
No Data Available
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References
No Data Available
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