240877

p-Toluenesulfonyl chloride

ReagentPlus®, ≥99%

Manufacturer: Sigma Aldrich

CAS Number: 98-59-9

Synonym(S): TsCl, Tosyl chloride

Select a Size

Pack Size SKU Availability Price
5 G 240877-5-G In Stock ₹ 5,074.55
100 G 240877-100-G In Stock ₹ 12,596.70
500 G 240877-500-G In Stock ₹ 38,971.70

240877 - 5 G

₹ 5,074.55

In Stock

Quantity

1

Base Price: ₹ 5,074.55

GST (18%): ₹ 913.419

Total Price: ₹ 5,987.969

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

Other Options

Image Product Name Manufacturer Price Range
50-269-5876
eMolecules​ Oakwood Chemical 4-Toluenesulfonyl chloride 100g 537723977 BR1703 98-59-9 MFCD00007450 190.640 C7H7ClO2S
eMolecules​ ₹ 3,116.95
NC2131738
eMolecules​ 4-Toluenesulfonyl chloride | 98-59-9 | MFCD00007450 | 500g
eMolecules​ ₹ 5,541.72
501839926
Sigma Aldrich Fine Chemicals Biosciences p-Toluenesulfonyl chloride | 98-59-9 | MFCD00007450 | 5 g
Sigma Aldrich Fine Chemicals Biosciences ₹ 6,382.78
501839924
Sigma Aldrich Fine Chemicals Biosciences p-Toluenesulfonyl chloride ReagentPlus(R), >=99% | 98-59-9 | MFCD00007450 | 100G
Sigma Aldrich Fine Chemicals Biosciences ₹ 14,673.54
T35955
p-Toluenesulfonyl chloride
Sigma Aldrich ₹ 2,289.35 - ₹ 8,091.85
8.08326
4-Toluenesulfonyl chloride
Sigma Aldrich ₹ 6,680.00 - ₹ 61,960.00
AB46947
98-59-9 | P-Toluenesulfonyl chloride
A2B Chem ₹ 684.48 - ₹ 3,935.76

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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: ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

SAFETY INFORMATION

Pictograms

GHS05,GHS07

Signal Word

Danger

Hazard Statements

H290,H315,H317,H318

Precautionary Statements

P280 - P302 + P352 - P305 + P351 + P338 + P310

Hazard Classifications

Eye Dam. 1 - Met. Corr. 1 - Skin Irrit. 2 - Skin Sens. 1

WGK

WGK 1

Flash Point(F)

262.4 °F

Flash Point(C)

128 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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benzene: freely soluble(lit.)chloroform: freely soluble(lit.)ethanol: freely soluble(lit.)water: insoluble(lit.)

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Cc1ccc(cc1)S(Cl)(=O)=O

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1S/C7H7ClO2S/c1-6-2-4-7(5-3-6)11(8,9)10/h2-5H,1H3

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