N-Ethynyl-4-methyl-N-(p-tolyl)benzenesulfonamide, 98%

Name: N-Ethynyl-4-methyl-N-(p-tolyl)benzenesulfonamide, 98% | 312329-87-6
Brand: J&K Chemical
SKU: JK9173618_1_G
Price: 84.8 USD
Availability: InStock

Cat. No JK9173618_1_G

Vendor: J&K Chemical

Product Information

Product Name

N-Ethynyl-4-methyl-N-(p-tolyl)benzenesulfonamide, 98%

Brand Name

J&K

Product Number

9173618

CAS

312329-87-6

Molecular Formula

C16H15NO2S

Molecular Weight

285.36

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

11369278

IUPAC Name

N-ethynyl-4-methyl-N-phenylbenzenesulfonamide

InChI Key

HFHLXBHDEWFCBC-UHFFFAOYSA-N

SMILES

CC1=CC=C(C=C1)S(=O)(=O)N(C#C)C2=CC=CC=C2

Safety Information

Storage Condition

Freezer -20℃

References Data Source From Pubchem

Alkynylation at Nitrogen

Publication Name: Science of Synthesis

Publication Date: 2025

Transition-Metal-Catalyzed Nucleophilic Dearomatization of Electron-Deficient Heteroarenes

Publication Name: Synthesis

Publication Date: 2021-09-09

DOI: 10.1055/a-1577-7638

Gold Carbenes Generated by Cycloisomerization of Alkynes and Alkenes

Publication Name: Science of Synthesis

Publication Date: 2017

Hay Coupling

Publication Name: Science of Synthesis

Publication Date: 2008

Synthesis of Disubstituted Ynamides from β,β-Dichloroenamides and Electrophiles

Publication Name: Synlett

Publication Date: 2007-07

DOI: 10.1055/s-2007-984529

N-Ethynyl-4-methyl-N-(p-tolyl)benzenesulfonamide, 98%

Product Information

General Information

Safety Information

References Data Source From Pubchem

Alkynylation at Nitrogen

Transition-Metal-Catalyzed Nucleophilic Dearomatization of Electron-Deficient Heteroarenes

Gold Carbenes Generated by Cycloisomerization of Alkynes and Alkenes

Hay Coupling

Synthesis of Disubstituted Ynamides from β,β-Dichloroenamides and Electrophiles