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4'-acetamidophenyl 4-phenyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133041-70-0 Structure
  • Basic information

    1. Product Name: 4'-acetamidophenyl 4-phenyl ether
    2. Synonyms: 4'-acetamidophenyl 4-phenyl ether
    3. CAS NO:133041-70-0
    4. Molecular Formula:
    5. Molecular Weight: 367.275
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133041-70-0.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: 4'-acetamidophenyl 4-phenyl ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4'-acetamidophenyl 4-phenyl ether(133041-70-0)
    11. EPA Substance Registry System: 4'-acetamidophenyl 4-phenyl ether(133041-70-0)
  • 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: 133041-70-0(Hazardous Substances Data)

133041-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133041-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,4 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133041-70:
(8*1)+(7*3)+(6*3)+(5*0)+(4*4)+(3*1)+(2*7)+(1*0)=80
80 % 10 = 0
So 133041-70-0 is a valid CAS Registry Number.

133041-70-0Relevant articles and documents

DNA-Direcred Alkylating Agents. 4. 4-Anilinoquinoline-Based Minor Groove Directed Aniline Mustards

Gravatt, G. Lance,Baguley, Bruce C.,Wilson, William R.,Denny, William A.

, p. 1552 - 1560 (2007/10/02)

A series of 4-anilinoquinoline-linked aniline mustards of widely varying mustard reactivity were prepared and evaluated for their antitumor activity.The compounds were designed as minor groove binding agents, where the aniline mustard ring is itself part of the DNA-binding ligand.While there was a general trend for cytotoxicity to correlate with mustard reactivity, this was much less pronounced than with untargeted mustards.The compounds were much more cytotoxic than the parent diols, and were also at least 10-fold more cytotoxic than the corresponding aniline mustards themselves.Comparative cell line studies suggested that the mechanism of cytotoxicity varied with mustard reactivity.The most reactive mustards cross-linked DNA, while cell killing by the less reactive compounds appeared to be by the formation of bulky monoadducts.The compounds were active but not particularly dose-potent against P388 leukemia in vivo.The modest potency may be related to their poor aqueous solubility, since the more soluble methyl quarternary salts were equally active at much lower doses.

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