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CAS

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106782-72-3

(E)-3-nitro-4'-acetoazobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 106782-72-3 Structure

  • Basic information

    1. Product Name: (E)-3-nitro-4'-acetoazobenzene
    2. Synonyms: (E)-3-nitro-4'-acetoazobenzene
    3. CAS NO:106782-72-3
    4. Molecular Formula:
    5. Molecular Weight: 269.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 106782-72-3.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: (E)-3-nitro-4'-acetoazobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-3-nitro-4'-acetoazobenzene(106782-72-3)
    11. EPA Substance Registry System: (E)-3-nitro-4'-acetoazobenzene(106782-72-3)

  • 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: 106782-72-3(Hazardous Substances Data)

106782-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106782-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,7,8 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106782-72:
(8*1)+(7*0)+(6*6)+(5*7)+(4*8)+(3*2)+(2*7)+(1*2)=133
133 % 10 = 3
So 106782-72-3 is a valid CAS Registry Number.

106782-72-3Relevant articles and documents

Design and synthesis of a photoswitchable guanidine catalyst

Viehmann, Philipp,Hecht, Stefan

, p. 1825 - 1830,6 (2012)

A novel design as well as a straight-forward synthesis for a photoswitchable guanidine catalyst is reported. Intense studies of the photochromic properties demonstrated the reversible switchability of its photosensitive azobenzene moiety. Its activity in

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