M-TOLUENESULFONYL CHLORIDE

M-TOLUENESULFONYL CHLORIDE Basic information
Product Name:M-TOLUENESULFONYL CHLORIDE
Synonyms:m-Toluenesulphonyl chloride, 98+%;3-(Chlorosulphonyl)toluene;m-Toluensulfonyl chloride;m-Tolylsulfonyl chloride;Toluene-3-sulfonyl chloride;3-Toluenesulfonyl chloride, 97% 5GR;3-Methylbenzenesulphonyl chloride 98%;3-TOLUENESULFONYL CHLORIDE
CAS:1899-93-0
MF:C7H7ClO2S
MW:190.65
EINECS:628-747-3
Product Categories:Organic Building Blocks;Sulfonyl Halides;Sulfur Compounds
Mol File:1899-93-0.mol
M-TOLUENESULFONYL CHLORIDE Structure
M-TOLUENESULFONYL CHLORIDE Chemical Properties
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. Inert atmosphere,Room Temperature
solubility Chloroform (Slightly), Ethyl Acetate (Slightly)
form liquid
color Clear, faint red to brown
Water Solubility Reacts with water.
Sensitive Moisture Sensitive
BRN 2087865
CAS DataBase Reference1899-93-0(CAS DataBase Reference)
Safety Information
Hazard Codes C
Risk Statements 34-29
Safety Statements 26-36/37/39-45
RIDADR UN 3265 8/PG 2
WGK Germany 3
Hazard Note Corrosive
HazardClass 8
PackingGroup II
HS Code 29049090
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
M-TOLUENESULFONYL CHLORIDE Usage And Synthesis
Chemical Propertiesclear yellow liquid
UsesReactant 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 Descriptionm-Toluenesulfonyl chloride can be synthesized via chlorination of m-thiocresol in glacial acetic acid.
M-TOLUENESULFONYL CHLORIDE Preparation Products And Raw materials
Preparation Products3-Methylbenzenesulfinic acid sodiuM salt-->3-Bromomethylbenzenesulfonyl chloride
3-(CHLOROSULFONYL)-4-METHOXYBENZOIC ACID α-Acetamido-p-toluenesulfonyl chloride 2-TOLUENESULFONYL CHLORIDE 98% 9,10-DIOXO-9,10-DIHYDROANTHRACENE-2-SULFONYL CHLORIDE 6-METHOXY-M-TOLUENESULFONYL CHLORIDE 4-TOLUENESULFONYL CHLORIDE [METHYL-14C] M-TOLUENESULFONYL CHLORIDE PENTAMETHYLBENZENESULFONYL CHLORIDE 3-NITRO-ALPHA-TOLUENESULFONYL CHLORIDE,3-Nitro-^a-toluenesulfonyl chloride, 95%,3-nitro-à-toluenesulfonyl chloride,3-Nitro-ɑ-toluenesulfonyl chloride, 95% 3,5-DICHLORO-ALPHA-TOLUENESULFONYL CHLORIDE 1,2-NAPHTHOQUINONE-2-DIAZIDO-5-SULFONYL CHLORIDE 2-nitro-α-toluenesulfonyl chloride,2-NITRO-ALPHA-TOLUENESULFONYL CHLORIDE 4-CHLORO-3-CHLOROSULFONYL-5-NITROBENZOIC ACID 4-Nitro-ɑ-toluenesulfonyl chloride, 97% α-bromo-p-toluenesulfonyl chloride,à-bromo-p-toluenesulfonyl chloride Sulfonylchloride polystyrene, p-Toluenesulfonyl chloride resin (1%DVB, 100-200 mesh, 0.5-4.0 mmol 4-Trifluoromethyl-ɑ-toluenesulfonyl chloride, 97% 2-chloro-5-(chlorosulfonyl)-benzoicaci

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