4-Bromo-2-methylanisole, 98%

Name: 4-Bromo-2-methylanisole, 98% | 14804-31-0
Brand: J&K Chemical
SKU: JKY08070_10_G
Price: 27.4 USD
Availability: OutOfStock

Cat. No JKY08070_10_G

Vendor: J&K Chemical

Product Information

Product Name

4-Bromo-2-methylanisole, 98%

Brand Name

J&K

Product Number

282292

CAS

14804-31-0

Molecular Formula

C8H9BrO

Molecular Weight

201.06

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

5-Bromo-2-methoxytoluene

PubChem CID

608315

IUPAC Name

4-bromo-1-methoxy-2-methylbenzene

InChI Key

UDLRGQOHGYWLCS-UHFFFAOYSA-N

SMILES

CC1=C(C=CC(=C1)Br)OC

Properties

Melting Point

66-69

Safety Information

Precautionary Statement

P262

References Data Source From Pubchem

Catalytic activation of unstrained C(aryl)–C(aryl) bonds in 2,2′-biphenols

Publication Name: Nature Chemistry

Publication Date: 2018-11-05

DOI: 10.1038/s41557-018-0157-x

Benzylic Amination via a Concerted Metalation–Deprotonation Process

Publication Name: Science of Synthesis

Publication Date: 2017

Ecofriendly Oxidative Nuclear Halogenation of Aromatic Compounds Using Potassium and Ammonium Halides

Publication Name: Synthesis

Publication Date: 2011-11-24

DOI: 10.1055/s-0031-1289620

Reductive Dehalogenation of Aryl Bromides and Chlorides and Their Use as Aryl Blocking Groups

Publication Name: Synthesis

Publication Date: 2009-11-13

DOI: 10.1055/s-0029-1217112

A convenient and selective method for the para-bromination of aromatic compounds with potassium bromide in the presence of poly(4-vinylpyridine)-supported peroxodisulfate in nonaqueous solution

Publication Name: Russian Journal of Organic Chemistry

Publication Date: 2007-09

DOI: 10.1134/s1070428007090047

4-Bromo-2-methylanisole, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Catalytic activation of unstrained C(aryl)–C(aryl) bonds in 2,2′-biphenols

Benzylic Amination via a Concerted Metalation–Deprotonation Process

Ecofriendly Oxidative Nuclear Halogenation of Aromatic Compounds Using Potassium and Ammonium Halides

Reductive Dehalogenation of Aryl Bromides and Chlorides and Their Use as Aryl Blocking Groups

A convenient and selective method for the para-bromination of aromatic compounds with potassium bromide in the presence of poly(4-vinylpyridine)-supported peroxodisulfate in nonaqueous solution