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Trimethylsulfoxonium iodide (1774-47-6)

Identification
Name:Trimethylsulfoxonium iodide
Synonyms:Trimethylsulphoxonium iodide
CAS:1774-47-6
EINECS: 217-204-2
Molecular Formula: C3H9IOS
Molecular Weight: 220.07
InChI: InChI=1/C3H9OS.HI/c1-5(2,3)4;/h1-3H3;1H/q+1;/p-1
Molecular Structure: (C3H9IOS) Trimethylsulphoxonium iodide
Properties
Transport:25kgs
Density:g/cm3
Stability:Stable under normal temperatures and pressures.
Appearance:white to yellow crystals
Specification:

With the CAS registry number 1774-47-6, Trimethyl sulphoxonium iodide is also named as Sulfonium, trimethyl-, iodide, oxide. The product's categories are iodonium sulfonium & oxonium compounds; sulfonium compounds; sulfur compounds (for synthesis); synthetic organic chemistry; sulfonium / sulfoxonium compounds; organic building blocks; sulfur compounds. It is white to light yellow crystalline powder which is sensitive to light. When heated to decomposition it emits toxic vapors of SOx and I-.

The other characteristics of this product can be summarized as:?(1)H-Bond Donor: 0; (2)H-Bond Acceptor: 2; (3)Rotatable Bond Count: 0; (4)Exact Mass: 219.941879; (5)MonoIsotopic Mass: 219.941879; (6)Topological Polar Surface Area: 18.1; (7)Heavy Atom Count: 6; (8)Complexity: 53.

Uses of?Trimethyl sulphoxonium iodide: It is mainly used for synthesis of fluconazole. And it also can be used in?organic synthesis. For example: 1.It reacts with?1-cyclohex-1-enyl-ethanone to get 1-acetylbicyclo[4.1.0]heptane. This reaction needs reagent?NaH and solvent?dimethylsulfoxide. The yield is 42%.



2.It also can react with?adamantan-2-one?to obtain?Adamantan-2-spiro-oxiran. This reaction needs reagent?NaOH?and solvent?propan-2-ol by heating. The reaction time is?1 hours. The yield is 85%.

When you are using this chemical, please be cautious about it as the following:
It is harmful if swallowed. And it is irritating to eyes, respiratory system and skin.?In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.?If you want to contact this product, you must wear suitable protective clothing, suitable gloves and eye/face protection.

People can use the following data to convert to the molecule structure.
1. SMILES: [I-].O=[S+](C)(C)C;
2. InChI: InChI=1/C3H9OS.HI/c1-5(2,3)4;/h1-3H3;1H/q+1;/p-1.

The following are the toxicity data which has been tested.

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 900mg/kg (900mg/kg) ? International Journal of Radiation Biology and Related Studies in Physics, Chemistry and Medicine. Vol. 3, Pg. 41, 1961.
mouse LD50 intravenous 180mg/kg (180mg/kg) ? U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#04108,

Report:

With the CAS registry number 1774-47-6, Trimethyl sulphoxonium iodide is also named as Sulfonium, trimethyl-, iodide, oxide. The product's categories are iodonium sulfonium & oxonium compounds; sulfonium compounds; sulfur compounds (for synthesis); synthetic organic chemistry; sulfonium / sulfoxonium compounds; organic building blocks; sulfur compounds. It is white to light yellow crystalline powder which is sensitive to light. When heated to decomposition it emits toxic vapors of SOx and I-.

The other characteristics of this product can be summarized as:?(1)H-Bond Donor: 0; (2)H-Bond Acceptor: 2; (3)Rotatable Bond Count: 0; (4)Exact Mass: 219.941879; (5)MonoIsotopic Mass: 219.941879; (6)Topological Polar Surface Area: 18.1; (7)Heavy Atom Count: 6; (8)Complexity: 53.

Uses of?Trimethyl sulphoxonium iodide: It is mainly used for synthesis of fluconazole. And it also can be used in?organic synthesis. For example: 1.It reacts with?1-cyclohex-1-enyl-ethanone to get 1-acetylbicyclo[4.1.0]heptane. This reaction needs reagent?NaH and solvent?dimethylsulfoxide. The yield is 42%.



2.It also can react with?adamantan-2-one?to obtain?Adamantan-2-spiro-oxiran. This reaction needs reagent?NaOH?and solvent?propan-2-ol by heating. The reaction time is?1 hours. The yield is 85%.

When you are using this chemical, please be cautious about it as the following:
It is harmful if swallowed. And it is irritating to eyes, respiratory system and skin.?In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.?If you want to contact this product, you must wear suitable protective clothing, suitable gloves and eye/face protection.

People can use the following data to convert to the molecule structure.
1. SMILES: [I-].O=[S+](C)(C)C;
2. InChI: InChI=1/C3H9OS.HI/c1-5(2,3)4;/h1-3H3;1H/q+1;/p-1.

The following are the toxicity data which has been tested.

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 900mg/kg (900mg/kg) ? International Journal of Radiation Biology and Related Studies in Physics, Chemistry and Medicine. Vol. 3, Pg. 41, 1961.
mouse LD50 intravenous 180mg/kg (180mg/kg) ? U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#04108,

HS Code: 29309070
Storage Temperature: Keep container closed when not in use. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. Store protected from light.
Sensitive: Light Sensitive
Safety Data
Hazard Symbols Xn:Harmful