Sigma-Aldrich 240877 p-Toluenesulfonyl chloride ReagentPlus®, ≥99% 100 gr
Category
Brand
Stock Code
LB.SA.240877-100G
Kısa Bilgi
Synonym(s): TsCl, Tosyl chloride Linear Formula: CH3C6H4SO2Cl CAS Number: 98-59-9 Molecular Weight: 190.65 Beilstein: 607898 EC Number: 202-684-8 MDL number: MFCD00007450 PubChem Substance ID: 57648053 NACRES: NA.21
| Sigma-Aldrich 240877 p-Toluenesulfonyl chloride ReagentPlus®, ≥99% 100 gr |
|
Synonym(s): TsCl, Tosyl chloride
Linear Formula: CH3C6H4SO2Cl
CAS Number: 98-59-9
Molecular Weight: 190.65
Beilstein: 607898
EC Number: 202-684-8
MDL number: MFCD00007450
PubChem Substance ID: 57648053
NACRES: NA.21 |
|
PROPERTIES
vapor pressure 1 mmHg ( 88 °C)
Quality Level 200
product line ReagentPlus®
Assay ≥99%
form solid
bp 134 °C/10 mmHg (lit.)
mp 65-69 °C (lit.)
solubility
benzene: freely soluble(lit.)
chloroform: freely soluble(lit.)
ethanol: freely soluble(lit.)
water: insoluble(lit.)
SMILES string Cc1ccc(cc1)S(Cl)(=O)=O
InChI 1S/C7H7ClO2S/c1-6-2-4-7(5-3-6)11(8,9)10/h2-5H,1H3
InChI key YYROPELSRYBVMQ-UHFFFAOYSA-N
DESCRIPTION
General description
p-Toluenesulfonyl chloride is an organic sulfonyl chloride mainly used to convert hydroxyl groups into good leaving group by forming sulfonates.[1]
Application
p-Toluenesulfonyl chloride may be used in the following processes:
- In combination with N-methylimidazole for the esterification or thioesterification of carboxylic acids and alcohols or thiols.[2]
- As an additive to enhance the yield of symmetrical biaryls via palladium chloride catalyzed homo-coupling of arylboronic acids in the absence of ligands.[3]
- As a positive chlorine source for the ?-chlorination of ketones.[4]
- Solvent-free tosylation of alcohols and phenols in the presence of heterodoxy acids.[5]
- As an activator for reaction between 2-alkynylbenzaldoxime and phenols to form 1-aroxyisoquinolines in the presence of silver triflate.[6]
As a catalyst for the solvent-free preparation of symmetrical bis(benzhydryl)ethers from benzhydrols.[7]
Legal Information
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