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2,6-dimethoxy-4-nitroaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 86955-74-0 Structure
  • Basic information

    1. Product Name: 2,6-dimethoxy-4-nitroaniline
    2. Synonyms: 2,6-dimethoxy-4-nitroaniline
    3. CAS NO:86955-74-0
    4. Molecular Formula:
    5. Molecular Weight: 198.178
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86955-74-0.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: 2,6-dimethoxy-4-nitroaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,6-dimethoxy-4-nitroaniline(86955-74-0)
    11. EPA Substance Registry System: 2,6-dimethoxy-4-nitroaniline(86955-74-0)
  • 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: 86955-74-0(Hazardous Substances Data)

86955-74-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86955-74-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,5 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86955-74:
(7*8)+(6*6)+(5*9)+(4*5)+(3*5)+(2*7)+(1*4)=190
190 % 10 = 0
So 86955-74-0 is a valid CAS Registry Number.

86955-74-0Relevant articles and documents

Potential antitumor agents. 39. Anilino ring geometry of amsacrine and derivatives: Relationship to DNA binding and antitumor activity

Denny,Atwell,Baguley

, p. 1625 - 1630 (1983)

The clinical antileukemic drug amsacrine and analogues are thought to exert their biological activity by binding tightly but reversibly to DNA, with the acridine chromophore intercalated and the anilino group making additional binding contact in the minor

Photoswitching Azo compounds in vivo with red light

Samanta, Subhas,Beharry, Andrew A.,Sadovski, Oleg,McCormick, Theresa M.,Babalhavaeji, Amirhossein,Tropepe, Vince,Woolley, G. Andrew

, p. 9777 - 9784 (2013/07/26)

The photoisomerization of azobenzenes provides a general means for the photocontrol of molecular structure and function. For applications in vivo, however, the wavelength of irradiation required for trans-to-cis isomerization of azobenzenes is critical si

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