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2,6-DIBROMO-1,5-DIHYDROXYNAPHTHALENE

  • CAS No.:84-59-3
  • Purity:99%
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Factory Export Top Purity 2,6-DIBROMO-1,5-DIHYDROXYNAPHTHALENE 84-59-3 In Stock

  • Molecular Formula:C10H6Br2O2
  • Molecular Weight:317.964
  • Vapor Pressure:6.92E-07mmHg at 25°C 
  • Melting Point:78-81?°C(lit.) 
  • Refractive Index:1.766 
  • Boiling Point:397.4 °C at 760 mmHg 
  • PKA:6.19±0.50(Predicted) 
  • Flash Point:194.2 °C 
  • PSA:40.46000 
  • Density:2.081 g/cm3 
  • LogP:3.77600 

2,6-DIBROMO-1,5-DIHYDROXYNAPHTHALENE(Cas 84-59-3) Usage

InChI:InChI=1/C10H6Br2O2/c11-7-3-1-5-6(10(7)14)2-4-8(12)9(5)13/h1-4,13-14H

84-59-3 Relevant articles

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Wheeler,Ergle

, p. 4872,4878 (1930)

-

Development of bulk heterojunction morphology by the difference of intermolecular interaction behaviors

Cha, Hyojung,Baek, Jang Yeol,An, Tae Kyu,Kim, Seul-Ong,Kwon, Soon-Ki,Kim, Yun-Hi,Park, Chan Eon

, p. 3558 - 3567 (2014)

The morphology of a bulk heterojunction ...

Synthesis and characterization of tetraoctyloxy substituted naphthalenophanedienes

Yu, Chin-Yang,Yu, Sheng-Hao,Wen, Shih-Hao,Wang, Chao-Chi

, p. 3854 - 3858 (2017)

Tetraoctyloxy-substituted naphthalenopha...

Convenient regioselective syntheses of isomeric bis(tetrathiafulvalenylethenyl)naphthalene π-donors

Gonzalez, Silvia,Martin, Nazario,Segura, Jose L.,Seoane, Carlos

, p. 3051 - 3054 (1998)

Novel highly soluble isomeric tetrathiaf...

From Colorless to Near-Infrared S-Heteroarene Isomers: Unexpected Cycloaromatization of Cyclopenta[ b]thiopyran Catalyzed by PtCl2

Lu, Yifan,Qiao, Yanjun,Xue, Haodong,Zhou, Gang

, p. 6632 - 6635 (2018)

S-heteroarenes containing cyclopenta[b]t...

Highly Fluorescent Red-Light Emitting Bis(boranils) Based on Naphthalene Backbone

Urban, Mateusz,Durka, Krzysztof,Jankowski, Piotr,Serwatowski, Janusz,Luliński, Sergiusz

, p. 8234 - 8241 (2017/08/14)

Ten bis(boranils) differently substitute...

84-59-3 Process route

1,5-dihydroxynaphthalene
83-56-7

1,5-dihydroxynaphthalene

2,6-dibromo-1,5-naphthalenediol
84-59-3

2,6-dibromo-1,5-naphthalenediol

Conditions
Conditions Yield
With bromine; In chloroform; at 0 - 20 ℃; for 3h;
89%
1,5-dihydroxynaphthalene; iodine; In acetic acid; at 80 ℃; Inert atmosphere;
With bromine; In acetic acid; for 12h; Reflux;
83%
With N-Bromosuccinimide; In N,N-dimethyl-formamide; acetonitrile; at 20 ℃;
80%
With bromine; iodine; acetic acid; at 70 ℃; for 1h;
80%
With bromine; iodine; In acetic acid; at 80 ℃;
77%
With bromine; acetic acid; at 80 ℃; for 2h; Inert atmosphere; Schlenk technique;
73%
With bromine; iodine; In acetic acid; at 80 ℃; for 0.5h;
57%
With bromine; iodine; In acetic acid; at 80 ℃; for 0.5h;
57%
With N-Bromosuccinimide; In acetonitrile; at 20 ℃; for 4h; Inert atmosphere;
16%
With bromine; iodine; acetic acid; at 80 ℃;
With bromine; In acetic acid; at 80 ℃;
With bromine; In acetic acid; Inert atmosphere; Heating;
With N-Bromosuccinimide;
1,5-dihydroxynaphthalene
83-56-7

1,5-dihydroxynaphthalene

bromine
7726-95-6

bromine

iodine
7553-56-2,12190-71-5,8031-47-8

iodine

acetic acid
64-19-7,77671-22-8

acetic acid

2,6-dibromo-1,5-naphthalenediol
84-59-3

2,6-dibromo-1,5-naphthalenediol

Conditions
Conditions Yield
at 80 ℃;

84-59-3 Upstream products

  • 83-56-7
    83-56-7

    1,5-dihydroxynaphthalene

  • 7726-95-6
    7726-95-6

    bromine

  • 7553-56-2
    7553-56-2

    iodine

  • 64-19-7
    64-19-7

    acetic acid

84-59-3 Downstream products

  • 91394-96-6
    91394-96-6

    2,6-dibromo-1,5-bis(methoxy)naphthalene

  • 93831-68-6
    93831-68-6

    9-bromo-3-(4-methoxyphenyl)naphtho<1,8-bc>pyran-2,6-dione

  • 93831-67-5
    93831-67-5

    5,9-dibromo-3-(4-methoxyphenyl)naphtho<1,8-bc>pyran-2,6-dione

  • 93831-65-3
    93831-65-3

    9-bromo-3-phenylnaphtho<1,8-bc>pyran-2,6-dione

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