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4-Chloro-3-iodophenol, a chemical compound with the molecular formula C6H4ClIO, is a white to light yellow crystalline powder. It is soluble in organic solvents such as ethanol and acetone. This versatile compound is known for its unique chemical properties, making it a valuable building block in the synthesis of various biologically active compounds.

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  • 202982-72-7 Structure
  • Basic information

    1. Product Name: 4-CHLORO-3-IODOPHENOL
    2. Synonyms: 4-CHLORO-3-IODOPHENOL;4-Chloro-1-hydroxy-3-iodobenzene
    3. CAS NO:202982-72-7
    4. Molecular Formula: C6H4ClIO
    5. Molecular Weight: 254.45
    6. EINECS: N/A
    7. Product Categories: Chlorine Compounds;Iodine Compounds
    8. Mol File: 202982-72-7.mol
  • Chemical Properties

    1. Melting Point: 75-77°C
    2. Boiling Point: 312.4°Cat760mmHg
    3. Flash Point: 142.7°C
    4. Appearance: /
    5. Density: 2.087g/cm3
    6. Vapor Pressure: 0.000288mmHg at 25°C
    7. Refractive Index: 1.677
    8. Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
    9. Solubility: N/A
    10. Sensitive: Light Sensitive
    11. CAS DataBase Reference: 4-CHLORO-3-IODOPHENOL(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-CHLORO-3-IODOPHENOL(202982-72-7)
    13. EPA Substance Registry System: 4-CHLORO-3-IODOPHENOL(202982-72-7)
  • Safety Data

    1. Hazard Codes: Xi,T
    2. Statements: 25-41
    3. Safety Statements: 26-39-45
    4. RIDADR: UN 2811 6.1 / PGIII
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 202982-72-7(Hazardous Substances Data)

202982-72-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-3-iodophenol is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Chloro-3-iodophenol is utilized as a precursor in the production of agrochemicals, helping to create compounds that can protect crops and enhance agricultural productivity.
Used in Chemical Research:
4-Chloro-3-iodophenol serves as a valuable building block in chemical research, enabling scientists to explore its reactivity and potential applications in creating novel compounds for various purposes.
Used in Research and Development Activities:
4-CHLORO-3-IODOPHENOL is also employed in research and development activities, where its unique properties are harnessed to innovate and discover new uses in medicine, agriculture, and other fields, further expanding its potential impact.

Check Digit Verification of cas no

The CAS Registry Mumber 202982-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,9,8 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 202982-72:
(8*2)+(7*0)+(6*2)+(5*9)+(4*8)+(3*2)+(2*7)+(1*2)=127
127 % 10 = 7
So 202982-72-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H4ClIO/c7-5-2-1-4(9)3-6(5)8/h1-3,9H

202982-72-7 Well-known Company Product Price

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  • Alfa Aesar

  • (B25547)  4-Chloro-3-iodophenol, 98%   

  • 202982-72-7

  • 1g

  • 425.0CNY

  • Detail
  • Alfa Aesar

  • (B25547)  4-Chloro-3-iodophenol, 98%   

  • 202982-72-7

  • 10g

  • 2447.0CNY

  • Detail

202982-72-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-CHLORO-3-IODOPHENOL

1.2 Other means of identification

Product number -
Other names 4-chloro-3-iodo-phenol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:202982-72-7 SDS

202982-72-7Relevant articles and documents

The Catalyst-Controlled Regiodivergent Chlorination of Phenols

Maddox, Sean M.,Dinh, Andrew N.,Armenta, Felipe,Um, Joann,Gustafson, Jeffrey L.

supporting information, p. 5476 - 5479 (2016/11/17)

Different catalysts are demonstrated to overcome or augment a substrate's innate regioselectivity. Nagasawa's bis-thiourea catalyst was found to overcome the innate para-selectivity of electrophilic phenol chlorination, yielding ortho-chlorinated phenols that are not readily obtainable via canonical electrophilic chlorinations. Conversely, a phosphine sulfide derived from 2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl (BINAP) was found to enhance the innate para-preference of phenol chlorination.

5,6-BISARYL-2-PYRIDINE-CARBOXAMIDE DERIVATIVES, PREPARATION AND APPLICATION THEREOF IN THERAPEUTICS AS UROTENSIN II RECEPTOR ANTAGONISTS

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Page/Page column 28, (2009/12/28)

The present invention relates to derivatives of 5,6-bisaryl-2-pyridine-carboxamide, their preparation and their application in therapeutics as antagonists of urotensin II receptors.

PYRROLE DERIVATIVE

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Page 73, (2010/02/06)

A novel pyrrole derivative represented by the following formula (1) and a salt thereof: wherein R1 means substituted alkenyl, etc.; R2 means substituted benzoyl, etc.; and R3 to R5 each means hydrogen, alkyl, halogeno, etc. The derivative and salt have antidiabetic activity.

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