1,3-dichloro-5-methylsulfanyl-benzene - Names and Identifiers
Name | 3,5-Dichloro thioanisole
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Synonyms | 3,5-DICHLOROTHIOANIS 3,5-DICHLOROTHIOANISOLE 3,5-Dichloro thioanisole 3,5-dichlorophenylmethylsulfide 3,5-Dichlorophenyl methyl sulfide 1,3-DICHLORO-5-(METHYLTHIO)BENZENE (3,5-dichlorophenyl)(methyl)sulfane 1,3-dichloro-5-methylsulfanylbenzene Benzene, 1,3-dichloro-5-(methylthio)- 1,3-dichloro-5-methylsulfanyl-benzene 1,3-Dichloro-5-(methylsulfanyl)benzene
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CAS | 68121-46-0
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InChI | InChI=1/C7H6Cl2S/c1-10-7-3-5(8)2-6(9)4-7/h2-4H,1H3 |
1,3-dichloro-5-methylsulfanyl-benzene - Physico-chemical Properties
Molecular Formula | C7H6Cl2S
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Molar Mass | 193.09 |
Density | 1.349g/mLat 25°C(lit.) |
Melting Point | 170-171 °C(Solv: benzene (71-43-2)) |
Boling Point | 262-263°C(lit.) |
Flash Point | >230°F |
Vapor Presure | 0.0365mmHg at 25°C |
Specific Gravity | 1.349 |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | n20/D 1.613(lit.) |
MDL | MFCD00870149 |
1,3-dichloro-5-methylsulfanyl-benzene - Risk and Safety
Hazard Symbols | Xi - Irritant
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Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin.
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Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
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WGK Germany | 3 |
Hazard Note | Irritant |
Hazard Class | IRRITANT, STENCH |
1,3-dichloro-5-methylsulfanyl-benzene - Introduction
3,5-Dichloro thioanisole is an organic compound with the chemical formula C7H4Cl2S. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: Colorless to light yellow liquid
-Solubility: Soluble in common organic solvents, such as ethanol, ether and chlorinated hydrocarbons
-melting point: about -55 ℃
-Boiling point: about 170-175 ℃
-Density: approx. 1.34g/cm³
-Composition analysis: Contains two chlorine atoms and one sulfur atom, with a spicy smell
Use:
- 3,5-Dichloro thioanisole can be used as reagents and intermediates in organic synthesis.
-It is commonly used in organic synthesis reactions to introduce sulfur groups, such as for the preparation of thioethers, thioureas and other sulfur-containing compounds.
Preparation Method:
- 3,5-Dichloro thioanisole is generally obtained by the reaction of anisol and chlorite. Chlorous gas reacts with anisol in ether solution to give 3,5-Dichloro thioanisole.
Safety Information:
- 3,5-Dichloro thioanisole are irritating and toxic and should avoid contact with skin, eyes and mucous membranes. Appropriate protective equipment such as gloves, goggles and face shields should be worn during use.
-It is also flammable and should be kept away from fire sources and stored in a sealed container away from direct sunlight.
-When handling or handling the compound, appropriate safety measures should be taken, and relevant safety operation procedures and regulations should be strictly observed.
Last Update:2024-04-10 22:29:15