| Identification | More | [Name]
M-TOLUENESULFONYL CHLORIDE | [CAS]
1899-93-0 | [Synonyms]
3-METHYLBENZENESULFONYL CHLORIDE
3-METHYLBENZENESULPHONYL CHLORIDE
3-TOLUENESULFONYL CHLORIDE
3-TOLUENESULPHONYL CHLORIDE
AKOS BBS-00006608
BENZENESULFONYL CHLORIDE, 3-METHYL-
M-TOLUENESULFONYL CHLORIDE
M-TOLUENESULPHONYL CHLORIDE
Dm-Toluenesulphonyl chloride
m-Toluenesulphonyl chloride, 98+% | [EINECS(EC#)]
628-747-3 | [Molecular Formula]
C7H7ClO2S | [MDL Number]
MFCD00051747 | [Molecular Weight]
190.65 | [MOL File]
1899-93-0.mol |
| Chemical Properties | Back Directory | [Appearance]
clear yellow liquid | [Melting point ]
108 °C | [Boiling point ]
252-253 °C (lit.) | [density ]
1.314 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.5490(lit.)
| [Fp ]
225 °F
| [storage temp. ]
Refrigerator (+4°C) | [Water Solubility ]
Reacts with water. | [Sensitive ]
Moisture Sensitive | [BRN ]
2087865 | [CAS DataBase Reference]
1899-93-0(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns.
R29:Contact with water liberates toxic gas. | [Safety Statements ]
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 label where possible) . | [RIDADR ]
UN 3265 8/PG 2
| [WGK Germany ]
3
| [Hazard Note ]
Corrosive | [HazardClass ]
8 | [PackingGroup ]
II | [HS Code ]
29049090 |
| Hazard Information | Back Directory | [Chemical Properties]
clear yellow liquid | [Uses]
Reactant involved in they synthesis of biologically active molecules including small molecule ligands for the Stat3 SH2 domain, aryldisulfonamides with antibacterial activity, quinazoline analogs for the treatment of Gaucher disease, 17β-HSD2 inhibitors for the treatment of osteoporosis, isoindoline-5-propenehydroxamates for use as histone deactylase inhibitors. | [General Description]
m-Toluenesulfonyl chloride can be synthesized via chlorination of m-thiocresol in glacial acetic acid. |
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