chlorophenylsulfone structure
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Common Name | chlorophenylsulfone | ||
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CAS Number | 98-09-9 | Molecular Weight | 176.621 | |
Density | 1.4±0.1 g/cm3 | Boiling Point | 251.5±9.0 °C at 760 mmHg | |
Molecular Formula | C6H5ClO2S | Melting Point | 14.5 °C | |
MSDS | Chinese USA | Flash Point | 105.9±18.7 °C | |
Symbol |
GHS05, GHS07, GHS08 |
Signal Word | Danger |
Name | Benzenesulfonyl Chloride |
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Synonym | More Synonyms |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 251.5±9.0 °C at 760 mmHg |
Melting Point | 14.5 °C |
Molecular Formula | C6H5ClO2S |
Molecular Weight | 176.621 |
Flash Point | 105.9±18.7 °C |
Exact Mass | 175.969879 |
PSA | 42.52000 |
LogP | 1.99 |
Vapour Pressure | 0.0±0.5 mmHg at 25°C |
Index of Refraction | 1.554 |
Stability | Stable. Incompatible with water, strong oxidizing agents, strong bases, methyl formamide, dimethyl sulfoxide. |
Water Solubility | may decompose |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
Symbol |
GHS05, GHS07, GHS08 |
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Signal Word | Danger |
Hazard Statements | H302 + H332-H314-H317-H334 |
Precautionary Statements | P261-P280-P305 + P351 + P338-P310 |
Personal Protective Equipment | Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | C:Corrosive |
Risk Phrases | R22;R29;R34 |
Safety Phrases | S23-S26-S36/37/39-S45 |
RIDADR | UN 2225 8/PG 3 |
WGK Germany | 1 |
RTECS | DB8750000 |
Packaging Group | III |
Hazard Class | 8 |
HS Code | 2904909090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2904909090 |
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Summary | HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0% |
Design, synthesis and structure-activity relationship studies of novel and diverse cyclooxygenase-2 inhibitors as anti-inflammatory drugs.
J. Enzyme Inhib. Med. Chem. 29(6) , 846-67, (2014) Because of the pivotal role of cyclooxygenase (COX) in the inflammatory processes, non-steroidal anti-inflammatory drugs (NSAIDs) that suppress COX activities have been used clinically for the treatme... |
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Design, synthesis, and bioevaluation of paeonol derivatives as potential anti-HBV agents.
Eur. J. Med. Chem. 90 , 428-35, (2015) Hepatitis B virus (HBV) is a causative reagent that frequently causes progressive liver diseases, leading to the development of acute, chronic hepatitis, cirrhosis, and eventually hepatocellular carci... |
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Comparison of manual and benzenesulfonyl chloride-semiautomated thiochrome methods for determination of thiamine in foods.
J. Assoc. Off. Anal. Chem. 64(3) , 616-22, (1981) A semiautomated procedure was used to measure the fluorescence of sample extracts before and after the addition of benzenesulfonyl chloride (BSC). Addition of BSC inhibited thiochrome formation and pr... |
Benzene sulfonyl chloride |
MFCD00007426 |
chlorophenylsulfone |
EINECS 202-636-6 |
Benzenesulfonic chloride |
Benzenesulfochloride |
Benzenesulfonyl chloride |
Phenylsulfonyl chloride |
Benzenesulphonyl chloride |
Benzenesulfonic acid chloride |