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ChemicalBook >> CAS DataBase List >>2-CHLORO-3-IODOPHENOL

2-CHLORO-3-IODOPHENOL

CAS No.
666727-31-7
Chemical Name:
2-CHLORO-3-IODOPHENOL
Synonyms
2-CHLORO-3-IODOPHENOL;Phenol, 2-chloro-3-iodo-
CBNumber:
CB7110915
Molecular Formula:
C6H4ClIO
Molecular Weight:
254.45
MDL Number:
MFCD08166415
MOL File:
666727-31-7.mol
MSDS File:
SDS
Last updated:2026-05-28 02:39:19
Product description Number Pack Size Price
2-Chloro-3-iodophenol 95% OR46706 100mg $166
2-Chloro-3-iodophenol 95% OR46706 250mg $320
2-Chloro-3-iodophenol 95% OR46706 500mg $475
2-Chloro-3-iodophenol 95% OR46706 1g $629
2-Chloro-3-iodophenol 97% AS110907 1g $105

2-CHLORO-3-IODOPHENOL Properties

storage temp. Keep in dark place,Sealed in dry,Room Temperature
Appearance Light brown to brown Solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319
Precautionary statements  P261-P305+P351+P338
HS Code  2908190090

2-CHLORO-3-IODOPHENOL price More Price(42)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Apolloscientific OR46706 2-Chloro-3-iodophenol 95% 666727-31-7 100mg $166 2026-06-04 Buy
Apolloscientific OR46706 2-Chloro-3-iodophenol 95% 666727-31-7 250mg $320 2026-06-04 Buy
Apolloscientific OR46706 2-Chloro-3-iodophenol 95% 666727-31-7 500mg $475 2026-06-04 Buy
Apolloscientific OR46706 2-Chloro-3-iodophenol 95% 666727-31-7 1g $629 2026-06-04 Buy
Activate Scientific AS110907 2-Chloro-3-iodophenol 97% 666727-31-7 1g $105 2026-06-04 Buy
Product number Packaging Price Buy
OR46706 100mg $166 Buy
OR46706 250mg $320 Buy
OR46706 500mg $475 Buy
OR46706 1g $629 Buy
AS110907 1g $105 Buy

2-CHLORO-3-IODOPHENOL Chemical Properties,Uses,Production

Synthesis

Phenol, 3-amino-2-chloro-

56962-01-7

2-CHLORO-3-IODOPHENOL

666727-31-7

The general procedure for the synthesis of 2-chloro-3-iodophenol from 3-amino-2-chlorophenol is as follows: 1. To a suspension of 2-amino-3-nitrophenol (10 g, 65 mmol) in concentrated hydrochloric acid (10 mL) was added dropwise an aqueous solution of sodium nitrite (5.1 g, 73.3 mmol) (60 mL) at 0 °C. After stirring for 30 min, 10% H2SO4 solution (3 mL) of CuCl (12.8 g, 130 mmol) was added and stirring was continued for 18 hours. The reaction mixture was filtered, washed with water and the filtrate was extracted with EtOAc (70 mL x 3). The EtOAc layer was concentrated to give 2-chloro-3-nitrophenol (7 g, 62% yield). 2. 2-Chloro-3-nitrophenol (6 g, 35 mmol) was dissolved in methanol (100 mL), ammonium chloride (9.4 g, 175.7 mmol) and zinc powder (46 g, 702.8 mmol) were added, and refluxed for 1 hour. It was filtered and concentrated to give 2-chloro-3-aminophenol (4.5 g, 90% yield) as a purple solid. 3. To a suspension of 2-chloro-3-aminophenol (4.5 g, 31 mmol) in concentrated hydrochloric acid (10 mL) was added an aqueous solution of sodium nitrite (2.5 g, 35 mmol) (50 mL) dropwise at 0 °C. After stirring for 30 min, 10% H2SO4 solution (3 mL) of iodine (10.4 g, 63 mmol) was added and stirred for 2 h at room temperature. After filtration, it was extracted with EtOAc and concentrated to give 2-chloro-3-iodophenol (6 g, 75% yield) as a dark purple solid. 4. 6-Bromo-2,2,4-trimethyl-1,2-dihydroquinoline (2.3 g, 9.2 mmol) was mixed with bis(pinacolato)diborane (4.2 g, 16.5 mmol) in DMSO (2 mL) and KOAc (2.7 g, 27.4 mmol) and PdCl2 (dppf) (100 mg) were added. The reaction was carried out at 120°C for 15 min in microwave, cooled and purified by chromatography to afford 2,2,4-trimethyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2-dihydroquinoline (2.3 g, 84% yield) as a white crystalline solid. 5. 2,2,4-Trimethyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2-dihydroquinoline (308 mg), 2-chloro-3-iodophenol (93 mg), PdCl2 (dppf) (100 mg) and KOAc (300 mg) were coupled to give 2-chloro-3-(2,2,4-trimethyl-1 ,2-dihydroquinolin-6-yl)phenol (85 mg). 6. The above product (85 mg) was reacted with NBS according to the method of Example 7 to obtain 3-(4-bromomethyl-2,2-dimethyl-1,2-dihydroquinolin-6-yl)-2-chlorophenol (56 mg). 7. Finally, the product (50 mg) was coupled with 2-phenylethanethiol (0.04 mL) to give the title compound (40 mg) as an oil.

References

[1] Patent: WO2004/18429, 2004, A2. Location in patent: Page 87

863870-84-2
666727-31-7
Synthesis of 2-CHLORO-3-IODOPHENOL from 2-CHLORO-3-IODOPHENYL N,N-DIETHYLCARBAMATE

2-CHLORO-3-IODOPHENOL Preparation Products And Raw materials

2-CHLORO-3-IODOPHENOL Suppliers

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2-CHLORO-3-IODOPHENOL Spectrum

2-CHLORO-3-IODOPHENOL Phenol, 2-chloro-3-iodo- 666727-31-7 C6H4ClIO pharmacetical
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