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1402921-30-5

2-tert-butyl-1-(2-chloro-4-nitrophenoxy)-4-methoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1402921-30-5 Structure

  • Basic information

    1. Product Name: 2-tert-butyl-1-(2-chloro-4-nitrophenoxy)-4-methoxybenzene
    2. Synonyms: 2-tert-butyl-1-(2-chloro-4-nitrophenoxy)-4-methoxybenzene
    3. CAS NO:1402921-30-5
    4. Molecular Formula:
    5. Molecular Weight: 335.787
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1402921-30-5.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-tert-butyl-1-(2-chloro-4-nitrophenoxy)-4-methoxybenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-tert-butyl-1-(2-chloro-4-nitrophenoxy)-4-methoxybenzene(1402921-30-5)
    11. EPA Substance Registry System: 2-tert-butyl-1-(2-chloro-4-nitrophenoxy)-4-methoxybenzene(1402921-30-5)

  • 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: 1402921-30-5(Hazardous Substances Data)

1402921-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1402921-30-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,9,2 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1402921-30:
(9*1)+(8*4)+(7*0)+(6*2)+(5*9)+(4*2)+(3*1)+(2*3)+(1*0)=115
115 % 10 = 5
So 1402921-30-5 is a valid CAS Registry Number.

1402921-30-5Downstream Products

1402921-30-5Relevant articles and documents

A fragment-based approach toward substituted trioxa[7]helicenes

Kelgtermans, Hans,Dobrzanska, Liliana,Dehaen, Wim,Van Meervelt, Luc

, p. 5200 - 5203,4 (2012)

A series of novel substituted trioxa[7]helicenes have been successfully prepared by a one-pot palladium catalyzed C-H arylation reaction starting from readily prepared dibenzofuran fragments. The dinitro-substituted helicene was analyzed by X-ray crystallography revealing the occurrence of two distinct enantiomers in the asymmetric unit, which forms interesting supramolecular motifs in the crystal, based on weak H-bonding interactions.

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