Catalog No.:AA00BBQV

2065-37-4 | 2-Bromonaphthalene-1,4-dione

Name: Name:2-Bromonaphthalene-1,4-dione
Brand: AABLOCKS
SKU: AA00BBQV
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250mg

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA00BBQV

Chemical Name:

2-Bromonaphthalene-1,4-dione

CAS Number:

2065-37-4

Molecular Formula:

C10H5BrO2

Molecular Weight:

237.0495

MDL Number:

MFCD00629301

SMILES:

O=C1C=C(Br)C(=O)c2c1cccc2

NSC Number:

401097

Properties

BP:

324.2°C at 760 mmHg

Form:

Solid

MP:

131-133°C(lit.)

Storage:

Inert atmosphere;Room Temperature;

Computed Properties

Complexity:

293

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

XLogP3:

2.4

Downstream Synthesis Route

74-93-1

2065-37-4

26037-62-7

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1954,vol.74,p.655 Chem.Abstr.,1954,p.10702

2065-37-4

4-Butyl-semicarbazid-hydrochlorid

17717-58-7

[1]ChemischeBerichte,1967,vol.100,p.3649-3654

530-48-3

2065-37-4

54988-91-9

[1]JournalofOrganicChemistry,1985,vol.50,p.52-60

[2]JournaloftheChemicalSociety.PerkinTransactions1(2001),2000,p.1149-1155

2065-37-4

5680-79-5

297749-73-6

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,p.5324-5328

2065-37-4

2491-20-5

methylN-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)-L-alaninate

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,p.5324-5328

Literature

Title: 2-Bromo-1,4-naphthoquinone: a potentially improved substitute of menadione in Apatone™ therapy.

Journal: Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 20120801

Title: On the search for potential anti-Trypanosoma cruzi drugs: synthesis and biological evaluation of 2-hydroxy-3-methylamino and 1,2,3-triazolic naphthoquinoidal compounds obtained by click chemistry reactions.

Journal: European journal of medicinal chemistry 20120601

Title: Cytotoxicity of naphthoquinones and their capacity to generate reactive oxygen species is quenched when conjugated with gold nanoparticles.

Journal: International journal of nanomedicine 20110101

Title: Bromide-sulfur interchange: ion chromatographic determination of total reduced thiol levels in plasma.

Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20080315

Title: Acaricidal activity and function of mite indicator using plumbagin and its derivatives isolated from Diospyros kaki Thunb. roots (Ebenaceae).

Journal: Journal of microbiology and biotechnology 20080201

Title: The 1,4-naphthoquinone scaffold in the design of cysteine protease inhibitors.

Journal: Bioorganic & medicinal chemistry 20070801

Title: Total synthesis of the proposed structure of the anthrapyran metabolite delta-indomycinone.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20070101

Title: Studies toward the total synthesis of angelmicin B (hibarimicin B): synthesis of a model CD-D' arylnaphthoquinone.

Journal: Organic letters 20041014

Title: Synthesis of 3-azido-2,3,6-trideoxy-beta-D-arabino-hexopyranosyl pyranonaphthoquinone analogues of medermycin.

Journal: Organic & biomolecular chemistry 20030521

Title: Quinonic derivatives active against Toxoplasma gondii.

Journal: Parasitology research 20021101

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SDS