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

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  • 90869-73-1 Structure
  • Basic information

    1. Product Name: 4-(tert-butyl)-2-chloronitrobenzene
    2. Synonyms: 4-(tert-butyl)-2-chloronitrobenzene
    3. CAS NO:90869-73-1
    4. Molecular Formula:
    5. Molecular Weight: 213.664
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90869-73-1.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: 4-(tert-butyl)-2-chloronitrobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(tert-butyl)-2-chloronitrobenzene(90869-73-1)
    11. EPA Substance Registry System: 4-(tert-butyl)-2-chloronitrobenzene(90869-73-1)
  • 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: 90869-73-1(Hazardous Substances Data)

90869-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90869-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,6 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90869-73:
(7*9)+(6*0)+(5*8)+(4*6)+(3*9)+(2*7)+(1*3)=171
171 % 10 = 1
So 90869-73-1 is a valid CAS Registry Number.

90869-73-1Downstream Products

90869-73-1Relevant articles and documents

Phenoxazine: A privileged scaffold for radical-trapping antioxidants

Farmer, Luke A.,Haidasz, Evan A.,Griesser, Markus,Pratt, Derek A.

, p. 10523 - 10536 (2017)

Diphenylamines are widely used to protect petroleum-derived products from autoxidation. Their efficacy as radical-trapping antioxidants (RTAs) relies on a balance of fast H-atom transfer kinetics and stability to one-electron oxidation by peroxidic specie

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