3-Phenoxypropyl bromide, 95%

Name: 3-Phenoxypropyl bromide, 95% | 588-63-6
Brand: J&K Chemical
SKU: JK265620_25_G
Price: 47.2 USD
Availability: OutOfStock

Cat. No JK265620_25_G

Vendor: J&K Chemical

Product Information

Product Name

3-Phenoxypropyl bromide, 95%

Brand Name

J&K

Product Number

265620

CAS

588-63-6

Molecular Formula

C9H11BrO

Molecular Weight

215.09

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

(3-Bromopropoxy)benzene
3-Phenoxypropyl bromide

PubChem CID

68522

IUPAC Name

3-bromopropoxybenzene

InChI Key

NIDWUZTTXGJFNN-UHFFFAOYSA-N

SMILES

C1=CC=C(C=C1)OCCCBr

Properties

Density

1.365

Melting Point

Boiling Point

130-134

Flash Point

n20D

1.5460

Safety Information

Precautionary Statement

P262

References Data Source From Pubchem

Decarboxylative Halogenation and Hydroxylation

Publication Name: Science of Synthesis

Publication Date: 2018

Novel substituted porphyrins: synthesis, characterization and photocatalytic activity of their TiO2-based composites

Publication Name: Journal of Inclusion Phenomena and Macrocyclic Chemistry

Publication Date: 2017-05-30

DOI: 10.1007/s10847-017-0724-6

Enantiomeric Separation of (R,S)-Aclidinium Bromide with Negatively Charged Gamma-Cyclodextrin by CE

Publication Name: Chromatographia

Publication Date: 2017-01-19

DOI: 10.1007/s10337-017-3244-z

Dodecanones

Publication Name: Aromatic Hydroxyketones: Preparation & Physical Properties

Publication Date: 2015

DOI: 10.1007/978-3-319-14185-5_10

Suzuki–Miyaura Cross-Coupling Reactions of Unactivated Alkyl Halides Catalyzed by a Nickel Pincer Complex

Publication Name: Synthesis

Publication Date: 2013-09-27

DOI: 10.1055/s-0033-1338544

3-Phenoxypropyl bromide, 95%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Decarboxylative Halogenation and Hydroxylation

Novel substituted porphyrins: synthesis, characterization and photocatalytic activity of their TiO2-based composites

Enantiomeric Separation of (R,S)-Aclidinium Bromide with Negatively Charged Gamma-Cyclodextrin by CE

Dodecanones

Suzuki–Miyaura Cross-Coupling Reactions of Unactivated Alkyl Halides Catalyzed by a Nickel Pincer Complex