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77197-98-9

4-nitro-2-cyclopropylphenyl 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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  • 77197-98-9 Structure

  • Basic information

    1. Product Name: 4-nitro-2-cyclopropylphenyl phenyl ether
    2. Synonyms:
    3. CAS NO:77197-98-9
    4. Molecular Formula:
    5. Molecular Weight: 255.273
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 77197-98-9.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: 4-nitro-2-cyclopropylphenyl phenyl ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-nitro-2-cyclopropylphenyl phenyl ether(77197-98-9)
    11. EPA Substance Registry System: 4-nitro-2-cyclopropylphenyl phenyl ether(77197-98-9)

  • 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: 77197-98-9(Hazardous Substances Data)

77197-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77197-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,9 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77197-98:
(7*7)+(6*7)+(5*1)+(4*9)+(3*7)+(2*9)+(1*8)=179
179 % 10 = 9
So 77197-98-9 is a valid CAS Registry Number.

77197-98-9Downstream Products

77197-98-9Relevant articles and documents

BEHAVIOR OF 2- AND 4-CYCLOPROPYLPHENYL ETHERS DURING NITRATION WITH NITRIC ACID IN ACETIC ANHYDRIDE

Mochalov, S. S.,Karpova, V. V.,Shabarov, Yu. S.

, p. 1780 - 1785 (2007/10/02)

During the nitration of 4-cyclopropyl phenyl ethers dilute nitric acid in acetic anhydride formal dealkylation (or dearylation) is realized with substituent entry of the nitro group into the para-substituted phenol which forms.Under analogous conditions the behavior of the corresponding ortho-substituted phenyl ethers depends both on the steric limitations created by the aroxyl (or alkoxyl) fragment and on its polar effect.In the reaction of cyclopropylphenyl ethers with concentrated nitric acid in acetic anhydride the formation of nitrophenols is hardly observed at all.

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