ChemicalBook > Product Catalog >Organic Chemistry >Alcohols,Phenols,Phenol alcohols >Phenol derivatives >4-Iodo-3-methyl-phenol

4-Iodo-3-methyl-phenol

4-Iodo-3-methyl-phenol Suppliers list
Company Name: Adamas Reagent, Ltd.  
Tel: 400-6009262 15618770481
Email: yhx@titansci.com
Company Name: Shanghai Harvest Chemical Industrial Co., Ltd.  
Tel: 15721252604 17321035817
Email: sales@harvest-chem.com
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Tel: 021-54306202 13764082696
Email: info@hanhongsci.com
Company Name: Shanghai Sunway Pharmaceutical Technology Co., Ltd  
Tel: 13761987713
Email: hxzheng@sunwaypharm.cn
Company Name: Wuhan ariel chemical Co., LTD.  
Tel: 18986259541 18986259541
Email: sales@3stc.com

4-Iodo-3-methyl-phenol manufacturers

  • 4-IODO-3-METHYL-PHENOL
  • 4-IODO-3-METHYL-PHENOL pictures
  • $1.30
  • 2024-10-22
  • CAS:133921-27-4
  • Min. Order: 1g
  • Purity: 98%
  • Supply Ability: 1kg,10kg,100kg
4-Iodo-3-methyl-phenol Basic information
Product Name:4-Iodo-3-methyl-phenol
Synonyms:3-methyl-4-iodophenol;4-Iodo-3-methyL;Phenol, 4-iodo-3-methyl-;4-Iodine-3-methylphenol;4-Iodo-3-methyl-phenol
CAS:133921-27-4
MF:C7H7IO
MW:234.03
EINECS:
Product Categories:
Mol File:133921-27-4.mol
4-Iodo-3-methyl-phenol Structure
4-Iodo-3-methyl-phenol Chemical Properties
Boiling point 276.7±28.0 °C(Predicted)
density 1.854±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka9.46±0.18(Predicted)
AppearanceOff-white to light brown Solid
Safety Information
MSDS Information
4-Iodo-3-methyl-phenol Usage And Synthesis
Synthesis
4-Amino-3-methylphenol

2835-99-6

4-IODO-3-METHYL-PHENOL

133921-27-4

Example 25: Synthesis of (E)-4-((2-(4-((Z)-1-(4-hydroxyphenyl)-2-phenylbut-1-en-1-yl)-3-methylphenoxy)ethyl)amino)-N,N-dimethylbut-2-enamide Step-1: Synthesis of 4-iodo-3-methylphenol 4-Amino-3-methylphenol (10 g, 81 mmol) was dissolved in THF (45 mL) and cooled to 0°C. Under stirring, 3M HCl (35 mL) was slowly added, followed by NaNO2 (6.1 g, 89 mmol), and the reaction was carried out for 10 min. Next, an aqueous solution of potassium iodide (53.89 g, 166 mmol) (140 mL) was added dropwise to the reaction mixture, and stirring was continued for 15 min by keeping 0°C. After completion of the reaction, the reaction mixture was extracted with EtOAc. The organic layer was washed with water and brine sequentially and concentrated under reduced pressure to obtain the crude product. The crude product was purified by silica gel column chromatography (230-400 mesh) to afford the title compound 4-iodo-3-methylphenol (9 g, 47% yield) using 10% EtOAc in hexane solution as eluent.

References[1] Patent: WO2016/196342, 2016, A1. Location in patent: Page/Page column 129
[2] Patent: US6689922, 2004, B1. Location in patent: Page column 85
[3] Journal of the Chemical Society, 1951, p. 1184,1186
[4] Patent: US6562823, 2003, B1
4-Iodo-3-methyl-phenol Preparation Products And Raw materials
Raw materials4-Amino-3-methylphenol-->m-Cresol-->Water-->Potassium iodide-->Sodium nitrite-->Tetrahydrofuran-->Hydrochloric acid
Tag:4-Iodo-3-methyl-phenol(133921-27-4) Related Product Information
4-Iodo-2-nitrophenol alpha-Ethyl-3-hydroxy-2,4,6-triiodohydrocinnamic acid 2,5-Dimethyl-4-iodophenol 3,5-Dimethyl-4-iodophenol 3-Hydroxy-2,4,6-triiodobenzoic acid 3-Iodo-4-methyl-phenol 4,5-Dimethoxy-2-iodobenzoic acid cicliomenol Methyl 2-iodo-5-hydroxybenzoate 5-Hydroxy-2-iodobenzoic acid SALOR-INT L134945-1EA AKOS AU36-M251 SALOR-INT L134899-1EA Iobutoic acid 2-Iodo-5,6-dimethoxybenzoic acid sodium salt 3-Hydroxy-2,4,6-triiodobenzoic acid, lithium salt (2-Iodo-5-methoxyphenyl)acetic acid 2-Iodo-5-methoxybenzoic acid