Details
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1.What is the 4-Iodophenol ?
Used in Organic Synthesis:
4-Iodophenol is used as a precursor in the field of organic synthesis for the production of various other compounds. Its unique structure and reactivity make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
4-Iodophenol is used as a starting material for the synthesis of certain pharmaceutical compounds. Its iodine atom can be replaced or modified in reactions, allowing for the creation of new drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
4-Iodophenol is used as a building block in the synthesis of agrochemicals, such as pesticides and herbicides. Its versatility in organic reactions enables the development of new and effective products for agricultural use.
Used in Specialty Chemicals:
4-Iodophenol is used as a key component in the production of specialty chemicals, including dyes, fragrances, and other industrial chemicals. Its ability to participate in a wide range of chemical reactions makes it a valuable asset in the synthesis of these diverse products.
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108-95-2,27073-41-2
phenol
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533-58-4
2-Iodophenol
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540-38-5
p-Iodophenol
| Conditions | Yield |
|---|---|
|
With
N-iodo-succinimide; toluene-4-sulfonic acid;
In
acetonitrile;
at 20 ℃;
for 14h;
regioselective reaction;
|
95%
4 %Chromat. |
|
With
Oxone; potassium iodide;
In
methanol;
at 20 ℃;
for 24h;
|
70%
24% |
|
With
[K(18-crown-6)]ICl2; calcium carbonate;
In
acetonitrile;
at 50 ℃;
regioselective reaction;
|
60%
12% |
|
With
iodine;
In
water;
Rate constant;
Product distribution;
Mechanism;
Ambient temperature;
in phosphate buffer containing I3(1-), pH=7.7 other pH, buffer and reactant concentration;
|
54%
8.8% |
|
With
KH2PO4 buffer; iodine; fipronilβ-cyclodextrin;
In
water;
Product distribution;
Ambient temperature;
var. buffer and pH, reaction without β-cyclodextrin; o-chlorophenol and aniline as substrates;
|
|
|
With
disodium hydrogenphosphate; potassium dihydrogenphosphate; iodine; fipronilβ-cyclodextrin; potassium iodide;
In
water;
at 25 ℃;
Kinetics;
Rate constant;
o-iodo-, p-iodo-, and o-chlorophenol as substrates; var. β-cyclodextrin concentration;
|
|
|
With
aluminum oxide; iodine;
In
solid;
for 20h;
Yield given. Yields of byproduct given;
Ambient temperature;
|
|
|
With
methanol; iodine; silver nitrate;
|
|
|
With
aluminium trichloride; cyanogen iodide;
In
diethyl ether; nitromethane;
at 25 ℃;
for 60h;
Yield given. Yields of byproduct given;
|
|
|
With
ferrocenium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate; Iodine monochloride; 2,3-dicyano-5,6-dichloro-p-benzoquinone;
In
dichloromethane;
at 20 ℃;
for 3h;
|
|
|
With
ferrocenium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate; Iodine monochloride; zinc(II) oxide;
In
dichloromethane;
at 20 ℃;
for 3h;
|
|
|
With
iodine; oxygen;
H5PV2Mo10O40;
In
[D3]acetonitrile;
at 80 ℃;
for 8h;
under 1520 Torr;
Title compound not separated from byproducts;
|
|
|
With
hydrogenchloride; potassium chlorate; potassium iodide;
In
methanol; water;
for 1h;
Title compound not separated from byproducts;
|
|
|
With
ammonium cerium(IV) nitrate; iodine;
at 20 ℃;
for 3.5h;
Title compound not separated from byproducts;
|
|
|
With
ammonium iodide; dihydrogen peroxide;
In
acetic acid;
at 20 ℃;
for 6h;
|
|
|
With
sodium persulfate; iodine; tertamethylammonium iodide;
In
acetonitrile;
at 80 ℃;
for 4h;
|
80 % Chromat.
18 % Chromat. |
|
With
dihydrogen peroxide; nitric acid; potassium iodide;
In
water; acetonitrile;
at 24.84 ℃;
for 4h;
under 760.051 Torr;
pH=Ca. 4;
regioselective reaction;
|
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phenol;
With
potassium iodide; sodium hydroxide;
In
water;
at 0 ℃;
for 0.333333h;
With
potassium ferrate(VI);
In
water;
at 20 ℃;
for 4h;
|
|
|
With
potassium ferrate(VI); iodine;
In
hexane;
for 2.33333h;
regioselective reaction;
Reflux;
|
|
|
With
sulfuric acid; dihydrogen peroxide; cetyltrimethylammonim bromide; sodium dodecyl-sulfate; potassium iodide;
In
water;
at 29.84 ℃;
for 2h;
Micellar solution;
|
|
|
With
sulfuric acid; iodine;
In
acetonitrile;
at 0 ℃;
for 0.5h;
Overall yield = 56 %; regioselective reaction;
Electrolysis;
|
|
|
With
iodine;
In
methanol;
at 28 ℃;
Temperature;
|
|
|
With
iodine; silver methanesulfonate;
In
acetonitrile;
at 23 ℃;
for 24h;
Overall yield = 80 percent; Overall yield = 35 mg;
|
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7553-56-2,12190-71-5,8031-47-8
iodine
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108-95-2,27073-41-2
phenol
-
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533-58-4
2-Iodophenol
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540-38-5
p-Iodophenol
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28177-54-0
2,6-diiodo-phenol
| Conditions | Yield |
|---|---|
|
With
dihydrogen peroxide;
In
methanol; water;
at 50 ℃;
for 2h;
under 760.051 Torr;
|
2.What is the CAS number for 4-Iodophenol ?
The CAS number of 4-Iodophenol is 540-38-5.
More information of 4-Iodophenol 540-38-5 are:
|
CAS?Number |
540-38-5 |
|
Density |
2.001 g/cm3 |
|
Melting Point |
92-94 °C(lit.) |
|
Boiling Point |
287.2 °C at 760 mmHg |
|
Flash Point |
112.4 °C |
|
Vapor Pressure |
0.00146mmHg at 25°C |
|
Refractive Index |
1.669 |
|
HS CODE |
29081900 |
|
PSA |
20.23000 |
|
LogP |
1.99680 |
3.What are another words for 4-Iodophenol ?
Synonyms?for?4-Iodophenol 540-38-5:Phenol,p-iodo- (6CI,8CI);1-Iodo-4-hydroxybenzene;4-Hydroxyiodobenzene;4-Hydroxyphenyl iodide;NSC 91464;p-Hydroxyiodobenzene;p-Iodophenol;
4.What is the molecular formula of 4-Iodophenol?
The chemical formula of ?4-Iodophenol is?C6H5IO which containing 6 Carbon atoms,5 Hydrogen atoms,1 Iodine atoms and 1 Oxygen atoms,and the molecular weight of??4-Iodophenol?is 220.01.
5.What is 4-Iodophenol (540-38-5) used for?
4-Iodophenol is an aromatic organic compound characterized by a phenol ring bonded with an iodine atom. It falls under the category of simple phenols and has the chemical formula C6H5IO. This solid substance is typically colorless to a very light pinkish color at room temperature. Due to its potential harmful effects when ingested, inhaled, or in contact with skin or eyes, it necessitates safe handling.
InChI:InChI=1/C6H5IO/c7-5-1-3-6(8)4-2-5/h1-4,8H
Relevant articles related to 4-Iodophenol:
|
Article |
Source |
|
Generation of Dimethyl Sulfoxide Coordinated Thermally Stable Halogen Cation Pools for C?H Halogenation |
Dalai, Pallaba Ganjan,Palit, Kuntal,Panda, Niranjan supporting information, p. 1031 - 1038 (2022/02/02) |
|
Ni-NiO heterojunctions: a versatile nanocatalyst for regioselective halogenation and oxidative esterification of aromatics |
Bhardwaj, Nivedita,Goel, Bharat,Indra, Arindam,Jain, Shreyans K.,Singh, Ajit Kumar,Tripathi, Nancy , p. 14177 - 14183 (2021/08/16) |
6.Buy 4-Iodophenol with the best price .
Xuzhou Long Yu Chemical Technology Co.Ltd is a quality supplier of 4-Iodophenol. Our main goal is customer satisfaction. Contact us to negotiate the best price for your business on 4-Iodophenol 540-38-5.
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