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CAS

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75850-36-1

1-phenyl-1-(2-phenoxyphenyl)propane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 75850-36-1 Structure

  • Basic information

    1. Product Name: 1-phenyl-1-(2-phenoxyphenyl)propane
    2. Synonyms:
    3. CAS NO:75850-36-1
    4. Molecular Formula:
    5. Molecular Weight: 288.389
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 75850-36-1.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: 1-phenyl-1-(2-phenoxyphenyl)propane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-phenyl-1-(2-phenoxyphenyl)propane(75850-36-1)
    11. EPA Substance Registry System: 1-phenyl-1-(2-phenoxyphenyl)propane(75850-36-1)

  • 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: 75850-36-1(Hazardous Substances Data)

75850-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75850-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,5 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75850-36:
(7*7)+(6*5)+(5*8)+(4*5)+(3*0)+(2*3)+(1*6)=151
151 % 10 = 1
So 75850-36-1 is a valid CAS Registry Number.

75850-36-1Downstream Products

75850-36-1Relevant articles and documents

SYNTHESIS AND TRANSFORMATIONS OF 2-CYCLOPROPYLPHENYL PHENYL SULFIDE AND 2-CYCLOPROPYLPHENYL PHENYL ETHER UNDER THE INFLUENCE OF AGENTS WITH ACIDIC CHARACTER

Shabarov, Yu. S.,Pisanova, E. V.,Saginova, L. G.

, p. 1218 - 1221 (2007/10/02)

2-Cyclopropylphenyl phenyl sulfide and 2-cyclopropylphenyl phenyl ether were synthesized from o-iodophenylcyclopropane by the Ullmann reaction.Treatment of the products with acidic agents gave products from their intramolecular self-alkylation, i.e., 9-et

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