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124782-67-8

2-(N-tert-butoxycarbonylamino)-4-fluoroanisole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124782-67-8 Structure

  • Basic information

    1. Product Name: 2-(N-tert-butoxycarbonylamino)-4-fluoroanisole
    2. Synonyms: 2-(N-tert-butoxycarbonylamino)-4-fluoroanisole
    3. CAS NO:124782-67-8
    4. Molecular Formula:
    5. Molecular Weight: 241.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124782-67-8.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: 2-(N-tert-butoxycarbonylamino)-4-fluoroanisole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(N-tert-butoxycarbonylamino)-4-fluoroanisole(124782-67-8)
    11. EPA Substance Registry System: 2-(N-tert-butoxycarbonylamino)-4-fluoroanisole(124782-67-8)

  • 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: 124782-67-8(Hazardous Substances Data)

124782-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124782-67-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,7,8 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 124782-67:
(8*1)+(7*2)+(6*4)+(5*7)+(4*8)+(3*2)+(2*6)+(1*7)=138
138 % 10 = 8
So 124782-67-8 is a valid CAS Registry Number.

124782-67-8Relevant articles and documents

4,5,6,7-trisubstituted benzoxazolones

-

, (2008/06/13)

Certain 6-aryl- or 6-heteroaryl- alkylaminobenzoxazolones, and their pharmaceutically-acceptable salts, are dual inhibitors of lipoxygenase and cyclooxygenase enzymes, and so are useful as antiallergy and antiinflammatory agents.

REGIOSPECIFIC SYNTHESIS OF CERTAIN 1,2,3,4-TETRASUBSTITUTED BENZENES IN ONE STEP VIA A BENZENE CYCLIZATION

Fisher, Lawrence E.,Caroon, Joan M.

, p. 233 - 238 (2007/10/02)

Tetrasubstituted benzenes of type 3 are obtained regiospecifically in a single step by the treatment of 1-fluoro-4-methoxy-5-carbo-tert-butoxy aniline with tert-butyllithium followed by reaction with an elecrophile.

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