14348-38-0
- Product Name：4-BROMO-3-HYDROXYBENZOIC ACID
- Molecular Formula：C7H5BrO3
- Purity：99%
- Molecular Weight：217.019
Product Details
Manufacturer supply high quality 4-BROMO-3-HYDROXYBENZOIC ACID 14348-38-0 with ISO standards
- Molecular Formula:C7H5BrO3
- Molecular Weight:217.019
- Vapor Pressure:3.77E-05mmHg at 25°C
- Melting Point:225-227 °C
- Refractive Index:1.654
- Boiling Point:338.644 °C at 760 mmHg
- PKA:3.85±0.10(Predicted)
- Flash Point:158.606 °C
- PSA：57.53000
- Density:1.862 g/cm3
- LogP:1.85290
4-BROMO-3-HYDROXYBENZOIC ACID(Cas 14348-38-0) Usage
InChI:InChI=1/C7H5BrO3/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,9H,(H,10,11)
14348-38-0 Relevant articles
Rim-functionalized cryptophane-111 derivatives via heterocapping, and their xenon complexes
Joseph, Akil I.,El-Ayle, Gracia,Boutin, Cline,Lonce, Estelle,Berthault, Patrick,Travis Holman
, p. 15905 - 15908 (2014)
Capping of cyclotriphenolene (3a) by the...
Synthesis of a triethylene glycol-capped benzo[1,2-c:4,5-c']bis[2]benzopyran-5,12-dione: A highly soluble dilactone-bridged p-terphenyl with a crankshaft architecture
Dressler, Justin J.,Charlesworth-Seiler, Eva M.,Dahl, Bart J.
, (2020)
3,10-Bis(triethylene glycol)benzo[1,2-c:...
The effect of carboxylate position on the structure of a metal organic framework derived from cyclotriveratrylene
Martin, Adam D.,Easun, Timothy L.,Argent, Stephen P.,Lewis, William,Blake, Alexander J.,Schr?der, Martin
, p. 603 - 607 (2017)
Two cyclotriveratrylene-based ligands H3...
Total Synthesis of Benzofuran-Based Aspergillusene B via Halogenative Aromatization of Enones
Bhatti, Aisha,Grabovyi, Gennadii A.,Mohr, Justin T.
supporting information, (2020/06/08)
A novel "non-aromatic pool" synthetic st...
Copper and L-(?)-quebrachitol catalyzed hydroxylation and amination of aryl halides under air
Bao, Xuefei,Chen, Guoliang,Dong, Jinhua,Du, Fangyu,Li, Hui,Liang, Xinjie,Wu, Ying,Zhang, Yongsheng
supporting information, (2020/08/03)
L-(?)-Quebrachitol, a natural product ob...
14348-38-0 Process route
-
-
64-19-7,77671-22-8
acetic acid
-
-
99-06-9
3-Carboxyphenol
-
-
14348-38-0
4-bromo-3-hydroxybenzoic acid
-
-
14348-40-4
2,4,6-tribromo-3-hydroxy-benzoic acid
-
-
14348-39-1
2,4-dibromo-5-hydroxybenzoic acid
| Conditions | Yield |
|---|---|
|
|
-
-
99-06-9
3-Carboxyphenol
-
-
14348-38-0
4-bromo-3-hydroxybenzoic acid
| Conditions | Yield |
|---|---|
|
With
bromine; acetic acid;
In
ethanol;
at 20 ℃;
for 0.5h;
|
52% |
|
With
bromine; acetic acid;
In
ethanol;
at 20 ℃;
for 0.5h;
|
40% |
|
With
bromine;
In
ethanol; acetic acid;
at 20 ℃;
for 0.5h;
|
40% |
|
With
bromine; acetic acid;
In
ethanol;
at 24 ℃;
for 0.5h;
|
40% |
|
With
bromine; acetic acid;
|
28% |
|
With
bromine;
In
acetic acid;
at 20 ℃;
for 120h;
|
28% |
|
With
bromine;
In
acetic acid;
|
21% |
|
With
bromine;
In
acetic acid;
|
21% |
|
With
bromine;
In
acetic acid;
at 20 ℃;
for 33h;
|
21% |
|
With
bromine;
In
water; acetic acid;
|
19% |
|
With
bromine; acetic acid;
at 18 - 22 ℃;
for 23h;
|
15.9% |
|
With
bromine; acetic acid;
at 20 ℃;
for 12h;
|
15% |
|
With
bromine; acetic acid;
|
12% |
|
With
bromine; acetic acid;
|
12% |
|
With
bromine; acetic acid;
|
|
|
With
bromine;
In
acetic acid;
|
|
|
With
bromine;
In
acetic acid;
|
|
|
With
bromine;
In
acetic acid;
|
|
|
With
bromine;
Inert atmosphere;
|
|
|
With
bromine; acetic acid;
|
|
|
With
carbon disulfide; bromine; iron(II) bromide;
|
|
|
With
tetrachloromethane; bromine; iron(II) bromide;
|
|
|
With
chloroform; bromine; iron(II) bromide;
|
|
|
With
bromine; acetic acid; iron(II) bromide;
|
|
|
With
bromine;
In
acetic acid;
at 0 ℃;
for 0.5h;
|
14348-38-0 Upstream products
-
99-06-9
3-Carboxyphenol
-
2374-03-0
4-aminosalicylic acid
-
22921-68-2
2-bromo-5-methoxy-benzoic acid
-
56-23-5
tetrachloromethane
14348-38-0 Downstream products
-
106291-80-9
methyl 4-bromo-3-hydroxybenzoate
-
79302-44-6
4-bromo-3-trimethylsiloxybenzoic acid trimethylsilyl ester
-
124318-23-6
3-Benzyloxy-4-brombenzoesaeure-benzylester
-
17054-27-2
4-bromo-3-benzyloxybenzoic acid
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