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100166-85-6

AURORA 306 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 100166-85-6 Structure

  • Basic information

    1. Product Name: AURORA 306
    2. Synonyms: AURORA 306;2-[2-(azepan-1-yl)-2-oxoethyl]-1H-isoindole-1,3(2H)-dione
    3. CAS NO:100166-85-6
    4. Molecular Formula: C16H18N2O3
    5. Molecular Weight: 286.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100166-85-6.mol

  • Chemical Properties

    1. Melting Point: 169.0-171.5 °C(Solv: ethyl acetate (141-78-6))
    2. Boiling Point: 477.6±28.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.271±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -0.92±0.20(Predicted)
    10. CAS DataBase Reference: AURORA 306(CAS DataBase Reference)
    11. NIST Chemistry Reference: AURORA 306(100166-85-6)
    12. EPA Substance Registry System: AURORA 306(100166-85-6)

  • 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: 100166-85-6(Hazardous Substances Data)

100166-85-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100166-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,6 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100166-85:
(8*1)+(7*0)+(6*0)+(5*1)+(4*6)+(3*6)+(2*8)+(1*5)=76
76 % 10 = 6
So 100166-85-6 is a valid CAS Registry Number.

100166-85-6Downstream Products

100166-85-6Relevant articles and documents

Photochemistry of ω-Phthalimidoalkanoic Acid Derivatives Syntheses of Multicyclic Fused Hydropyrazines and 1,4-Diazepines

Takechi, Haruko,Machida, Minoru,Kanaoka,Yuichi

, p. 859 - 868 (2007/10/02)

Photochemical reactions of phthalimides having various carbonyl functions (amides 3a-h, esters 11,14, and thioester 17) in their N-alkyl side chain are studied.By irradiation fused hydropyrazines (4a, e, g, h) and hydro-1,4-diazepines (4b, f) were formed from amide derivatives 3 through photocyclization, whereas the esters 11,14 showed addition and reduction reactions of the imide carbonyl group, and thioester 17 showed Norrish-type I reaction of the thioester moiety, in each case, however, without yielding cyclized products.

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