2,6-Dichlorostyrene, 98%

Name: 2,6-Dichlorostyrene, 98% | 28469-92-3
Brand: J&K Chemical
SKU: JK363515_5_G
Price: 149.0 USD
Availability: OutOfStock

Cat. No JK363515_5_G

Vendor: J&K Chemical

Product Information

Product Name

2,6-Dichlorostyrene, 98%

Brand Name

J&K

Product Number

363515

CAS

28469-92-3

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

34254

IUPAC Name

1,3-dichloro-2-ethenylbenzene

InChI Key

YJCVRMIJBXTMNR-UHFFFAOYSA-N

SMILES

C=CC1=C(C=CC=C1Cl)Cl

Safety Information

Storage Condition

Store at 2-8℃

References Data Source From Pubchem

A general photocatalytic platform for the regio- and stereoselective β-chloroacylation of alkenes and alkynes using a heteroleptic copper(I) complex

Publication Name: Nature Catalysis

Publication Date: 2025-06-24

DOI: 10.1038/s41929-025-01357-y

Alkoxyhalogenation of Dichlorostyrenes in Unsaturated C3-Alcohols

Publication Name: Russian Journal of Organic Chemistry

Publication Date: 2020-01

DOI: 10.1134/s1070428020010066

Iodosulfonylation of Alkenes Followed by Dehydroiodination

Publication Name: Science of Synthesis

Publication Date: 2018

Tosylmethyl Isocyanide and Alkenes

Publication Name: Science of Synthesis

Publication Date: 2013

An Efficient Synthesis of Vinyl Sulfones from Alkenes and Aryl Sulfinates¹

Publication Name: Synthesis

Publication Date: 2011-07-28

DOI: 10.1055/s-0030-1260142

2,6-Dichlorostyrene, 98%

Product Information

General Information

Safety Information

References Data Source From Pubchem

A general photocatalytic platform for the regio- and stereoselective β-chloroacylation of alkenes and alkynes using a heteroleptic copper(I) complex

Alkoxyhalogenation of Dichlorostyrenes in Unsaturated C3-Alcohols

Iodosulfonylation of Alkenes Followed by Dehydroiodination

Tosylmethyl Isocyanide and Alkenes

An Efficient Synthesis of Vinyl Sulfones from Alkenes and Aryl Sulfinates¹