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36161-26-9

Phenol, 4-fluoro-, potassium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 36161-26-9 Structure

  • Basic information

    1. Product Name: Phenol, 4-fluoro-, potassium salt
    2. Synonyms:
    3. CAS NO:36161-26-9
    4. Molecular Formula: C6H5FO.K
    5. Molecular Weight: 150.194
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 36161-26-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Phenol, 4-fluoro-, potassium salt(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phenol, 4-fluoro-, potassium salt(36161-26-9)
    11. EPA Substance Registry System: Phenol, 4-fluoro-, potassium salt(36161-26-9)

  • 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: 36161-26-9(Hazardous Substances Data)

36161-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36161-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,6 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36161-26:
(7*3)+(6*6)+(5*1)+(4*6)+(3*1)+(2*2)+(1*6)=99
99 % 10 = 9
So 36161-26-9 is a valid CAS Registry Number.

36161-26-9Upstream product

36161-26-9Relevant articles and documents

(2-Fluoroallyl)palladium complexes as intermediates in Pd-catalyzed Tsuji-Trost 2-fluoroallylations: Synthesis and reactivity

Bobrova, Angelina Yu.,Mezentsev, Igor A.,Novikov, Maxim A.,Tomilov, Yury V.

, (2020)

The first examples of π-(2-fluoroallyl)palladium complexes were synthesized, isolated and characterized including chloride dimers, neutral chloride or cationic triflate complexes bearing PPh3 or SPhos as the ligands. Preliminary reactivity patterns indicating strong dependence of the chemoselectivity on “hardness” of the nucleophile and the ligand type were studied.

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