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ChemicalBook >> CAS DataBase List >>4-Iodophenol

4-Iodophenol

CAS No.
540-38-5
Chemical Name:
4-Iodophenol
Synonyms
P-IODOPHENOL;4-lodophenoI;p-Jodphenol;p-iodo-pheno;4-IODOPHENOL;4-iodo-pheno;Phenol, p-iodo-;PHENOL, 4-IODO-;4-Iodophenol99%;PARA-IODOPHENOL
CBNumber:
CB8328252
Molecular Formula:
C6H5IO
Molecular Weight:
220.01
MDL Number:
MFCD00002327
MOL File:
540-38-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-04 16:00:12
Product description Number Pack Size Price
4-Iodophenol 99% I10201 10g $72
4-Iodophenol 99% I10201 25g $113
4-Iodophenol >98.0%(GC) I0311 10g $50
4-Iodophenol >98.0%(GC) I0311 25g $95
4-Iodophenol TRC-I717510-50G 50g $288
More product size

4-Iodophenol Properties

Melting point 92-94 °C(lit.)
Boiling point 138 °C5 mm Hg(lit.)
Density 1.8573
Flash point 138°C/5mm
storage temp. Refrigerator
solubility Chloroform (Slightly), Methanol (Slightly)
form Crystals or Crystalline Powder
pka 9.33(at 25℃)
color Pink or beige to brown
Water Solubility slightly soluble
Sensitive Light Sensitive
Merck 14,5036
BRN 1904544
Henry's Law Constant 4.6×101 mol/(m3Pa) at 25℃, Hilal et al. (2008)
Stability Stable. Incompatible with strong oxidizing agents.
InChI 1S/C6H5IO/c7-5-1-3-6(8)4-2-5/h1-4,8H
InChIKey VSMDINRNYYEDRN-UHFFFAOYSA-N
SMILES Oc1ccc(I)cc1
CAS DataBase Reference 540-38-5(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII BH194BAK0B
NIST Chemistry Reference Phenol, 4-iodo-(540-38-5)
EPA Substance Registry System p-Iodophenol (540-38-5)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Environment (GHS09)
GHS07,GHS09
Signal word  Warning
Hazard statements  H315-H319-H411
Precautionary statements  P501-P273-P264-P280-P302+P352-P391-P337+P313-P305+P351+P338-P362+P364-P332+P313
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  C,Xi,Xn
Risk Statements  21/22-34-36/37/38-20/21/22
Safety Statements  26-36/37/39-45-22
RIDADR  UN 3261 8/PG 3
WGK Germany  3
RTECS  SL5600000
Hazard Note  Irritant
TSCA  TSCA listed
HazardClass  IRRITANT, LACHRYMATOR
HS Code  29081900
Storage Class 8A - Combustible corrosive hazardous materials
Hazard Classifications Acute Tox. 4 Oral
Skin Corr. 1B
Limited Quantities 5.0 kg (11 lbs) (solid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L)
NFPA 704
1
3 1

4-Iodophenol price More Price(87)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich I10201 4-Iodophenol 99% 540-38-5 10g $72 2026-04-30 Buy
Sigma-Aldrich I10201 4-Iodophenol 99% 540-38-5 25g $113 2026-04-30 Buy
TCI Chemical I0311 4-Iodophenol >98.0%(GC) 540-38-5 10g $50 2026-04-30 Buy
TCI Chemical I0311 4-Iodophenol >98.0%(GC) 540-38-5 25g $95 2026-04-30 Buy
TRC TRC-I717510-50G 4-Iodophenol 540-38-5 50g $288 2026-06-03 Buy
Product number Packaging Price Buy
I10201 10g $72 Buy
I10201 25g $113 Buy
I0311 10g $50 Buy
I0311 25g $95 Buy
TRC-I717510-50G 50g $288 Buy

4-Iodophenol Chemical Properties,Uses,Production

Chemical Properties

Light brown powder. It dissolves slightly in water, but readily dissolves in ethanol, ether, and other organic solvents.

Uses

4-Iodophenol is used in chemiluminescence imaging assays and experiments, as diagnostic agents in order to detect cancer cells in patients. It is also utilized in synthesizing agonists for the estrogen β receptor. Additionally, The compound finds extensive applications in various medical industries as well as in human and animal nutrition products such as pharmaceutical intermediates, and polarizing films for Liquid Crystal Display (LCD) chemicals.

Preparation

It is obtained from 4-Aminophenol by diazotisation and substitution.

Application

4-Iodophenol can be used as a building block for the synthesis of:
Hydroxybiaryls by reacting with aryl boronic acids via Pd-catalyzed Suzuki-Miyaura coupling reaction.[1][2]
Aryl substituted olefins by reacting with acrylates via Pd-catalyzed Heck reaction.[3]
Iodinated-4-aryloxymethylcoumarins [4]
Hydroxylated stilbenoids [5] and psammaplysenes A and B.[6]

Definition

ChEBI: 4-iodophenol is an iodophenol.

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 2, p. 355, 1943
The Journal of Organic Chemistry, 70, p. 8590, 2005 DOI: 10.1021/jo051191x
Tetrahedron Letters, 40, p. 6051, 1999 DOI: 10.1016/S0040-4039(99)01236-8

Metabolism

4-Iodophenol has known human metabolites that include (2S,3S,4S,5R)-3,4,5-trihydroxy-6-(4-iodophenoxy)oxane-2-carboxylic acid.

Purification Methods

Crystallise 4-iodophenol from pet ether (b 80-100o) or distil it in vacuo. If the material has a brown or violet color, then dissolve it in CHCl3, shake it with 5% sodium thiosulfate solution until is colourless. Dry (Na2SO4), extract, evaporate and disil the residue in vacuo. [Dains & Eberly Org Synth Coll Vol II 355 1948, Beilstein 6 IV 1074.]

References

[1] HIDEHIRO SAKURAI Toshikazu H Tatsuya Tsukuda. Pd/C as a Reusable Catalyst for the Coupling Reaction of Halophenols and Arylboronic Acids in Aqueous Media[J]. The Journal of Organic Chemistry, 2002, 67 8: 2721-2722. DOI:10.1021/jo016342k.
[2] PIOTR WAWRZYNIAK Joachim H. Microwave-Promoted Suzuki—Miyaura Coupling of Arylboronic Acids with 1-Bromo-2-naphthol, o-Bromophenol, and o-Chlorophenol.[J]. ChemInform, 2007, 38 14. DOI:10.1002/chin.200714105.
[3] LUNXIANG YIN Juergen L. Carbon—Carbon Coupling Reactions Catalyzed by Heterogeneous Palladium Catalysts[J]. ChemInform, 2007, 38 22. DOI:10.1002/chin.200722237.
[4] MAHANTESHA BASANAGOUDA . Synthesis, structure–activity relationship of iodinated-4-aryloxymethyl-coumarins as potential anti-cancer and anti-mycobacterial agents[J]. European Journal of Medicinal Chemistry, 2014, 74: Pages 225-233. DOI:10.1016/j.ejmech.2013.12.061.
[5] AMIT SHARD. Tandem Heck/Decarboxylation/Heck Strategy: Protecting-Group-Free Synthesis of Symmetric and Unsymmetric Hydroxylated Stilbenoids[J]. Angewandte Chemie International Edition, 2012, 51 49: 12250-12253. DOI:10.1002/anie.201206346.
[6] SAVVAS N. GEORGIADES Jon C. Total Synthesis of Psammaplysenes A and B, Naturally Occurring Inhibitors of FOXO1a Nuclear Export[J]. Organic Letters, 2005, 7 19: 4091-4094. DOI:10.1021/ol0513286.

5122-99-6
540-38-5
Synthesis of 4-Iodophenol from 4-Iodophenylboronic acid
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View Lastest Price from 4-Iodophenol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
4-Iodophenol pictures 2026-07-09 4-Iodophenol
540-38-5
$1.00-100.00 1KG 99% Henan Fengda Chemical Co., Ltd
4-Iodophenol pictures 2025-06-20 4-Iodophenol
540-38-5
1kg 99.00% 20tons Hebei Yanxi Chemical Co., Ltd.
4-Iodophenol pictures 2021-07-13 4-Iodophenol
540-38-5
$10.00-15.00 1KG 99%+ HPLC Zhuozhou Wenxi import and Export Co., Ltd
  • 4-Iodophenol pictures
  • 4-Iodophenol
    540-38-5
  • $1.00-100.00
  • 99%
  • Henan Fengda Chemical Co., Ltd
  • 4-Iodophenol pictures
  • 4-Iodophenol
    540-38-5
  • $0.00
  • 99.00%
  • Hebei Yanxi Chemical Co., Ltd.
  • 4-Iodophenol pictures
  • 4-Iodophenol
    540-38-5
  • $10.00-15.00
  • 99%+ HPLC
  • Zhuozhou Wenxi import and Export Co., Ltd
4-hydroxyiodobenzene 4-hydroxyphenyliodide 4-iodo-pheno Phenol, p-iodo- p-hydroxyiodobenzene p-iodo-pheno PHENOL, 4-IODO- 4-IODOPHENOL p-Iodophenol 4-Iodophenol 4-Iodophenol99% 4-Iodophenol, 98+% PARA-IODOPHENOL p-hydroxyiodobenzen p-Jodphenol Phenol to iodine 4-Iodophenol, 99% 10GR 4-Iodophenol, 99% 25GR 4-Iodophenol [for BiocheMical Research] I**4-Iodophenol 4-Iodophenol> 4-Iodophenol[forBiochemicalResearch]> 4-Iodophenol, ≥ 98.0% 2-cyclopropyl-7-methyl-2,4,9,15-tetraazatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaen-10-one 4-lodophenoI P-IODOPHENOL 540-38-5 129681-40-2 C6H5IO ALCOHOL Building Blocks Organic Building Blocks Oxygen Compounds Phenols Pyridines Building Blocks C6 to C8 Chemical Synthesis Organic Building Blocks Oxygen Compounds Aromatic Phenols Phenol&Thiophenol&Mercaptan Phenoles and thiophenoles Heterocyclic Compounds Organic Building Blocks Oxygen Compounds Phenols
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