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912343-40-9

(3-chloro-5-iodophenyl)methanol is a chemical compound characterized by the molecular formula C7H6ClIO and a molecular weight of 284.48 g/mol. It is a derivative of phenylmethanol, featuring chlorine and iodine substituents on the phenyl ring. (3-chloro-5-iodophenyl)methanol is recognized for its versatile reactivity and compatibility with various functional groups, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, dyes, pigments, and specialty chemicals. The unique combination of chlorine and iodine in its molecular structure endows it with potential applications in medicinal chemistry and drug development, where it can serve as a building block for designing novel molecules with pharmacological properties.

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  • 912343-40-9 Structure

  • Basic information

    1. Product Name: (3-chloro-5-iodophenyl)methanol
    2. Synonyms: (3-chloro-5-iodophenyl)methanol;3-CHLORO-5-IODOBENZYL ALCOHOL
    3. CAS NO:912343-40-9
    4. Molecular Formula: C7H6ClIO
    5. Molecular Weight: 268.47941
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 912343-40-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (3-chloro-5-iodophenyl)methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-chloro-5-iodophenyl)methanol(912343-40-9)
    11. EPA Substance Registry System: (3-chloro-5-iodophenyl)methanol(912343-40-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 912343-40-9(Hazardous Substances Data)

912343-40-9 Usage

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
(3-chloro-5-iodophenyl)methanol is utilized as an intermediate in the production of various pharmaceuticals and agrochemicals, capitalizing on its reactivity and functional group compatibility to facilitate the synthesis of diverse compounds with therapeutic or pesticidal properties.
Used in Dye and Pigment Production:
(3-chloro-5-iodophenyl)methanol is also employed in the creation of dyes and pigments, where its unique molecular structure contributes to the development of specialty chemicals with specific color and stability characteristics.
Used in Medicinal Chemistry and Drug Development:
(3-chloro-5-iodophenyl)methanol holds promise in medicinal chemistry and drug development as a building block for generating new classes of molecules with potential pharmacological activities, thanks to its chlorine and iodine substituents that allow for the introduction of a wide range of functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 912343-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,3,4 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 912343-40:
(8*9)+(7*1)+(6*2)+(5*3)+(4*4)+(3*3)+(2*4)+(1*0)=139
139 % 10 = 9
So 912343-40-9 is a valid CAS Registry Number.

912343-40-9Relevant articles and documents

2-(1,2,3-TRIAZOL-2-YL)BENZAMIDE AND 3-(1,2,3-TRIAZOL-2-YL)PICOLINAMIDE DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS

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Paragraph 0447; 0448, (2015/06/17)

The present invention relates to 2-(1,2,3-triazol-2-yl)benzamide and 3-(1,2,3-triazol-2-yl)picolinamide derivatives of formula (I) wherein Ar1, Q, and R1 to R5 are as described in the description, to their preparation, to

2-(1,2,3-TRIAZOL-2-YL)BENZAMIDE AND 3-(1,2,3-TRIAZOL-2-YL)PICOLINAMIDE DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 60; 61, (2013/05/23)

The present invention relates to 2-(1,2,3-triazol-2-yl)benzamide and 3-(1,2,3-triazol-2- yl)picolinamide derivatives of formula (I) Formula (I) wherein Ar1, Q, and R1 to R5 are as described in the description, to their pre

SUBSTITUTED BENZYLIMIDAZOLES USEFUL FOR THE TREATMENT OF INFLAMMATORY DISEASES

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Page/Page column 81-82, (2008/06/13)

The invention comprises a class of derivatives of substituted benzylimidazoles of the formula (I) and methods for making the same. These compounds are useful for the treatment of inflammatory conditions.

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