Octyl 4-methylbenzenesulfonate, 96%

Name: Octyl 4-methylbenzenesulfonate, 96% | 3386-35-4
Brand: J&K Chemical
SKU: JK514318_25_G
Price: 26.2 USD
Availability: OutOfStock

Cat. No JK514318_25_G

Vendor: J&K Chemical

Product Information

Product Name

Octyl 4-methylbenzenesulfonate, 96%

Brand Name

J&K

Product Number

514318

CAS

3386-35-4

Molecular Formula

C15H24O3S

Molecular Weight

284.41

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

n-Octyl p-Toluenesulfonate

PubChem CID

599296

IUPAC Name

octyl 4-methylbenzenesulfonate

InChI Key

LYQJBZLAANNIER-UHFFFAOYSA-N

SMILES

CCCCCCCCOS(=O)(=O)C1=CC=C(C=C1)C

Properties

Density

1.06

Flash Point

191

Safety Information

Storage Condition

Room temperature

References Data Source From Pubchem

Transition-Metal-Catalyzed Carboxylation of Organic Halides and Their Surrogates with Carbon Dioxide

Publication Name: Synthesis

Publication Date: 2017-09-13

DOI: 10.1055/s-0036-1590908

Using Ammonium Fluorides or Hydrogen Difluorides

Publication Name: Science of Synthesis

Publication Date: 2017

Reaction of Arene- or Methanesulfonates with the Ionic Liquid 1-Butyl-3-methylimidazolium Bromide

Publication Name: Science of Synthesis

Publication Date: 2017

Using Difluorosilicate Derivatives

Publication Name: Science of Synthesis

Publication Date: 2017

Using Potassium Fluoride

Publication Name: Science of Synthesis

Publication Date: 2017

Octyl 4-methylbenzenesulfonate, 96%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Transition-Metal-Catalyzed Carboxylation of Organic Halides and Their Surrogates with Carbon Dioxide

Using Ammonium Fluorides or Hydrogen Difluorides

Reaction of Arene- or Methanesulfonates with the Ionic Liquid 1-Butyl-3-methylimidazolium Bromide

Using Difluorosilicate Derivatives

Using Potassium Fluoride