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916068-36-5

N,N’-diisopropylindoline-1-carboximidamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 916068-36-5 Structure

  • Basic information

    1. Product Name: N,N’-diisopropylindoline-1-carboximidamide
    2. Synonyms: N,N’-diisopropylindoline-1-carboximidamide
    3. CAS NO:916068-36-5
    4. Molecular Formula:
    5. Molecular Weight: 245.368
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 916068-36-5.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: N,N’-diisopropylindoline-1-carboximidamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N’-diisopropylindoline-1-carboximidamide(916068-36-5)
    11. EPA Substance Registry System: N,N’-diisopropylindoline-1-carboximidamide(916068-36-5)

  • 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: 916068-36-5(Hazardous Substances Data)

916068-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 916068-36-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,0,6 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 916068-36:
(8*9)+(7*1)+(6*6)+(5*0)+(4*6)+(3*8)+(2*3)+(1*6)=175
175 % 10 = 5
So 916068-36-5 is a valid CAS Registry Number.

916068-36-5Downstream Products

916068-36-5Relevant articles and documents

Titanacarborane mediated C-N bond forming/breaking reactions

Shen, Hao,Xie, Zuowei

scheme or table, p. 1652 - 1657 (2009/10/11)

Constrained-geometry titanacarboranes [σ:η1:η5-(OCH2)(R2NCH2)C2B9H9]Ti(NR2) (R = Me, Et) are synthesized via an unexpected reaction of [Me3NH][μ-7,8-CH2OCH2-7,8-C2B9H10] with Ti(NR2)4 (R = Me, Et), involving a C-O bond cleavage and C-N bond formation. These complexes can be readily converted to new amide species or alkoxide by reacting with amines or esters, respectively. Insertion of a series of unsaturated molecules into the Ti-N bond of the aforementioned complexes results in the formation of various half-sandwich titanacarboranes. [σ:η1:η5-(OCH2)(Me2NCH2)C2B9H9]Ti(NMe2) is also able to efficiently catalyze the hydroamination of carbodiimides and the transamination of guanidines. These results are summarized in this brief account.

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