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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
-
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
-
-
83-56-7
1,5-dihydroxynaphthalene
-
-
84-59-3
2,6-dibromo-1,5-naphthalenediol
| 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;
|
-
-
83-56-7
1,5-dihydroxynaphthalene
-
-
7726-95-6
bromine
-
-
7553-56-2,12190-71-5,8031-47-8
iodine
-
-
64-19-7,77671-22-8
acetic acid
-
-
84-59-3
2,6-dibromo-1,5-naphthalenediol
| Conditions | Yield |
|---|---|
|
at 80 ℃;
|
84-59-3 Upstream products
-
83-56-7
1,5-dihydroxynaphthalene
-
7726-95-6
bromine
-
7553-56-2
iodine
-
64-19-7
acetic acid
84-59-3 Downstream products
-
91394-96-6
2,6-dibromo-1,5-bis(methoxy)naphthalene
-
93831-68-6
9-bromo-3-(4-methoxyphenyl)naphtho<1,8-bc>pyran-2,6-dione
-
93831-67-5
5,9-dibromo-3-(4-methoxyphenyl)naphtho<1,8-bc>pyran-2,6-dione
-
93831-65-3
9-bromo-3-phenylnaphtho<1,8-bc>pyran-2,6-dione
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