氯甲酰基硫氯
chlorocarbonylsulfenyl chloride
CAS: 2757-23-5
Molecular Formula: CCl2OS
氯甲酰基硫氯 - Names and Identifiers
氯甲酰基硫氯 - Physico-chemical Properties
| Molecular Formula | CCl2OS |
| Molar Mass | 130.98 |
| Density | 1.552 g/mL at 25 °C (lit.) |
| Boling Point | 98 °C (lit.) |
| Flash Point | 98-101°C |
| Vapor Presure | 40.7mmHg at 25°C |
| Appearance | Liquid, Fuming In Moist Air |
| Color | Yellow |
| BRN | 506318 |
| Storage Condition | 2-8°C |
| Sensitive | Moisture Sensitive |
| Refractive Index | n20/D 1.517(lit.) |
氯甲酰基硫氯 - Risk and Safety
| Hazard Symbols | C - Corrosive |
| Risk Codes | R34 - Causes burns R37 - Irritating to the respiratory system |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| UN IDs | UN 3265 8/PG 2 |
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 9-13-21 |
| HS Code | 29309090 |
| Hazard Class | 8 |
| Packing Group | II |
氯甲酰基硫氯 - Introduction
chlorocarbonylsulfenyl chloride is an organic compound with the chemical formula ClCOSCl. It is a colorless liquid with a pungent pungent odor. The following is a description of the nature, use, formulation and safety information of chlorocarbonylsulfenyl chloride:
Nature:
1. Appearance: colorless liquid
2. Odor: spicy pungent odor
3. Density: 1.587g/cm³
4. Boiling point: 82-84 ° C
5. Melting point:-35 ° C
6. Solubility: Soluble in some organic solvents, such as ether and dichloromethane
Use:
1. As an intermediate in Organic Synthesis: chlorocarbonylsulfonyl chloride is often used as a synthetic intermediate of organic compounds and is used to prepare other organic compounds, such as acylation reagents, acetone urea compounds, etc.
2. As acylation reagent: chlorocarbonylsulfenyl chloride can be used for acylation reaction, and react with alcohol or amine to generate corresponding ester or amide.
Method:
The common preparation methods of chlorocarbonylsulfenyl chloride include the following two:
1. Oxidation method: the precursor of chlorocarbonylsulphenyl chloride (thionyl chloride) reacts with chlorine gas to generate chlorocarbonylsulphenyl chloride.
2. Chlorination method: reacting carbon thionyl chloride with sulfonyl chloride to generate chlorocarbonylsulfonyl chloride.
Safety Information:
chlorocarbonylsulfenyl chloride is corrosive and irritating, so when using and operating, you need to pay attention to the following safety precautions:
1. Avoid contact with skin, eyes and respiratory tract. If necessary, wear chemical protective gloves, goggles and appropriate protective masks.
2. Use in well ventilated conditions, avoid inhalation of steam. It can be operated in a chemical laboratory or under a dedicated fume hood.
3. Store away from fire and heat sources, avoid high temperature and direct sunlight.
4. Use and handle in strict accordance with relevant regulations and operating specifications, and avoid contact with incompatible substances to avoid dangerous reactions.
Please note that the use of chemical substances must follow the correct safety procedures, and under the guidance of experienced personnel.
Nature:
1. Appearance: colorless liquid
2. Odor: spicy pungent odor
3. Density: 1.587g/cm³
4. Boiling point: 82-84 ° C
5. Melting point:-35 ° C
6. Solubility: Soluble in some organic solvents, such as ether and dichloromethane
Use:
1. As an intermediate in Organic Synthesis: chlorocarbonylsulfonyl chloride is often used as a synthetic intermediate of organic compounds and is used to prepare other organic compounds, such as acylation reagents, acetone urea compounds, etc.
2. As acylation reagent: chlorocarbonylsulfenyl chloride can be used for acylation reaction, and react with alcohol or amine to generate corresponding ester or amide.
Method:
The common preparation methods of chlorocarbonylsulfenyl chloride include the following two:
1. Oxidation method: the precursor of chlorocarbonylsulphenyl chloride (thionyl chloride) reacts with chlorine gas to generate chlorocarbonylsulphenyl chloride.
2. Chlorination method: reacting carbon thionyl chloride with sulfonyl chloride to generate chlorocarbonylsulfonyl chloride.
Safety Information:
chlorocarbonylsulfenyl chloride is corrosive and irritating, so when using and operating, you need to pay attention to the following safety precautions:
1. Avoid contact with skin, eyes and respiratory tract. If necessary, wear chemical protective gloves, goggles and appropriate protective masks.
2. Use in well ventilated conditions, avoid inhalation of steam. It can be operated in a chemical laboratory or under a dedicated fume hood.
3. Store away from fire and heat sources, avoid high temperature and direct sunlight.
4. Use and handle in strict accordance with relevant regulations and operating specifications, and avoid contact with incompatible substances to avoid dangerous reactions.
Please note that the use of chemical substances must follow the correct safety procedures, and under the guidance of experienced personnel.
Last Update：2024-04-10 22:29:15
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Product Name: Chlorocarbonylsulfenyl Chloride Visit Supplier Webpage Request for quotationCAS: 2757-23-5
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922
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Product Name: Chlorocarbonylsulfenyl Chloride Visit Supplier Webpage Request for quotationCAS: 2757-23-5
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View History
氯甲酰基硫氯
73501-08-3
Cyclohexadecanecarbonitrile, 1-(1-ethoxyethoxy)-
ETHYL 3-AMINO-5-(2,4-DICHLORO-5-FLUOROPHENYL)THIOPHENE-2-CARBOXYLATE
2-Amino-7-azaspiro[3.5]nonane-7-carboxylic acid tert-butyl ester
2-(3-甲氧基苯基)丙酸乙酯
1-(3,5-dichloro-2,6-dihydroxy-4-methoxyphenyl)hexan-1-one
ETHYL 1-(4-PHENYLTHIAZOL-2-YL)-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLATE
Dispersant
tert-butyl 3-(2-aminopyrimidin-4-yl)piperidine-1-carboxylate
73501-08-3
Cyclohexadecanecarbonitrile, 1-(1-ethoxyethoxy)-
ETHYL 3-AMINO-5-(2,4-DICHLORO-5-FLUOROPHENYL)THIOPHENE-2-CARBOXYLATE
2-Amino-7-azaspiro[3.5]nonane-7-carboxylic acid tert-butyl ester
2-(3-甲氧基苯基)丙酸乙酯
1-(3,5-dichloro-2,6-dihydroxy-4-methoxyphenyl)hexan-1-one
ETHYL 1-(4-PHENYLTHIAZOL-2-YL)-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLATE
Dispersant
tert-butyl 3-(2-aminopyrimidin-4-yl)piperidine-1-carboxylate