5-Bromoacenaphthene, 95%

Name: 5-Bromoacenaphthene, 95% | 2051-98-1
Brand: J&K Chemical
SKU: JK405844_5_G
Price: 66.9 USD
Availability: OutOfStock

Cat. No JK405844_5_G

Vendor: J&K Chemical

Product Information

Product Name

5-Bromoacenaphthene, 95%

Brand Name

J&K

Product Number

405844

CAS

2051-98-1

Molecular Formula

C12H9Br

Molecular Weight

233.11

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

74923

IUPAC Name

5-bromo-1,2-dihydroacenaphthylene

InChI Key

QALKJGMGKYKMKE-UHFFFAOYSA-N

SMILES

C1CC2=CC=C(C3=CC=CC1=C23)Br

Properties

Melting Point

54-56

Boiling Point

335

Flash Point

>113

References Data Source From Pubchem

New Bromine-Containing Bis(arylimino)acenaphthenes and Related Metal Complexes

Publication Name: Russian Journal of Coordination Chemistry

Publication Date: 2020-04-11

DOI: 10.1134/s1070328420030045

Nitroacenaphthene as a New Photocatalyst for the Synthesis of Sulfonyl Amidines

Publication Name: Synthesis

Publication Date: 2019-09-13

DOI: 10.1055/s-0039-1690984

Synthesis of Aromatic Carboxylic Acids by Carbonylation of Aryl Halides in the Presence of Epoxide-Modified Cobalt Carbonyls as Catalysts

Publication Name: Russian Journal of Applied Chemistry

Publication Date: 2005-11

DOI: 10.1007/s11167-005-0619-y

Using a Preformed Grignard Reagent

Publication Name: Science of Synthesis

Publication Date: 2003

Perylene derivatives formation in reaction of 3-bromobenzanthrone and 4-bromonaphthalic acid derivatives with a reduction system NiCl2-2,2′bipyridyl (or 1,10-phenathroline)-Zn

Publication Name: Russian Journal of Electrochemistry

Publication Date: 2000-06

DOI: 10.1007/bf02757446

5-Bromoacenaphthene, 95%

Product Information

General Information

Properties

References Data Source From Pubchem

New Bromine-Containing Bis(arylimino)acenaphthenes and Related Metal Complexes

Nitroacenaphthene as a New Photocatalyst for the Synthesis of Sulfonyl Amidines

Synthesis of Aromatic Carboxylic Acids by Carbonylation of Aryl Halides in the Presence of Epoxide-Modified Cobalt Carbonyls as Catalysts

Using a Preformed Grignard Reagent

Perylene derivatives formation in reaction of 3-bromobenzanthrone and 4-bromonaphthalic acid derivatives with a reduction system NiCl2-2,2′bipyridyl (or 1,10-phenathroline)-Zn