2-Iodo-m-xylene, 98%

Name: 2-Iodo-m-xylene, 98% | 608-28-6
Brand: J&K Chemical
SKU: JK239282_5_G
Price: 124.0 USD
Availability: InStock

Cat. No JK239282_5_G

Vendor: J&K Chemical

Product Information

Product Name

2-Iodo-m-xylene, 98%

Brand Name

J&K

Product Number

239282

CAS

608-28-6

Molecular Formula

C8H9I

Molecular Weight

232.06

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

2-Iodo-1,3-dimethylbenzene

PubChem CID

69097

IUPAC Name

2-iodo-1,3-dimethylbenzene

InChI Key

QTUGGVBKWIYQSS-UHFFFAOYSA-N

SMILES

CC1=C(C(=CC=C1)C)I

Properties

Melting Point

Boiling Point

223-224

Flash Point

102

n20D

1.6010-1.6050

Safety Information

GHS Symbols

Signal Word

Danger

Hazard Statement

H315

H318

H335

Precautionary Statement

P280

P321

P261

P271

P319

P405

P501

P302+P352

P332+P317

P362+P364

P264+P265

P305+P354+P338

P304+P340

P403+P233

References Data Source From Pubchem

Mapping the mechanisms of oxidative addition in cross-coupling reactions catalysed by phosphine-ligated Ni(0)

Publication Name: Nature Chemistry

Publication Date: 2024-02-14

DOI: 10.1038/s41557-024-01451-x

Transition-Metal-Free C(sp)—C(sp2) Cross-Coupling Reactions

Publication Name: Science of Synthesis

Publication Date: 2024

Recent Advances to Mediate Reductive Processes of Nitroarenes Using Single-Electron Transfer, Organomagnesium, or Organozinc Reagents

Publication Name: Synthesis

Publication Date: 2022-05-30

DOI: 10.1055/a-1792-6579

Arylation of nitromethane with sterically hindered aryl halides

Publication Name: Russian Chemical Bulletin

Publication Date: 2022-01

DOI: 10.1007/s11172-022-3376-7

C—O Bond-Forming Reactions Involving Phenols

Publication Name: Science of Synthesis

Publication Date: 2022

2-Iodo-m-xylene, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Mapping the mechanisms of oxidative addition in cross-coupling reactions catalysed by phosphine-ligated Ni(0)

Transition-Metal-Free C(sp)—C(sp2) Cross-Coupling Reactions

Recent Advances to Mediate Reductive Processes of Nitroarenes Using Single-Electron Transfer, Organomagnesium, or Organozinc Reagents

Arylation of nitromethane with sterically hindered aryl halides

C—O Bond-Forming Reactions Involving Phenols

2-Iodo-m-xylene, 98%

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

About Us

Popular Searches

Contact

#title#

Features
Availability:
Price
Options
Actions

2-Iodo-m-xylene, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Mapping the mechanisms of oxidative addition in cross-coupling reactions catalysed by phosphine-ligated Ni(0)

Transition-Metal-Free C(sp)—C(sp2) Cross-Coupling Reactions

Recent Advances to Mediate Reductive Processes of Nitroarenes Using Single-Electron Transfer, Organomagnesium, or Organozinc Reagents

Arylation of nitromethane with sterically hindered aryl halides

C—O Bond-Forming Reactions Involving Phenols

2-Iodo-m-xylene, 98%

Related Product

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

#title#

Login

Register