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110966-08-0

N,N-Diisopropyl-3-phenylaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 110966-08-0 Structure

  • Basic information

    1. Product Name: N,N-Diisopropyl-3-phenylaniline
    2. Synonyms: N,N-Diisopropyl-3-phenylaniline
    3. CAS NO:110966-08-0
    4. Molecular Formula:
    5. Molecular Weight: 253.387
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 110966-08-0.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: N,N-Diisopropyl-3-phenylaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-Diisopropyl-3-phenylaniline(110966-08-0)
    11. EPA Substance Registry System: N,N-Diisopropyl-3-phenylaniline(110966-08-0)

  • 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: 110966-08-0(Hazardous Substances Data)

110966-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110966-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,9,6 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 110966-08:
(8*1)+(7*1)+(6*0)+(5*9)+(4*6)+(3*6)+(2*0)+(1*8)=110
110 % 10 = 0
So 110966-08-0 is a valid CAS Registry Number.

110966-08-0Downstream Products

110966-08-0Relevant articles and documents

Thermal and Photochemical Electron-Transfer Reactions of 4-Chlorobiphenyl with Lithium Diisopropylamides and Diisopropylamine

Tanaka, Yoshio,Tsujimoto, Kazuo,Ohashi, Mamoru

, p. 788 - 790 (1987)

A reaction of 4-chlorobiphenyl with lithium diisopropylamide in a polar solvent gave 3- and 4-(diisopropylamino)biphenyl together with biphenyl, similar to the case of photoinduced reactions of 4-chlorobiphenyl with diisopropylamine.A common electron-transfer mechanism is proposed.

The anionic thia-Fries rearrangement of aryl triflates

Charmant, Jonathan P. H.,Dyke, Alan M.,Lloyd-Jones, Guy C.

, p. 380 - 381 (2007/10/03)

Aryl triflates undergo LDA-mediated rearrangement to generate o-hydroxyaryl trifluoromethylsulfones. In some cases, partitioning between rearrangement and aryne generation can be controlled.

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