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C27H28N2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 116585-41-2 Structure
  • Basic information

    1. Product Name: C27H28N2
    2. Synonyms:
    3. CAS NO:116585-41-2
    4. Molecular Formula:
    5. Molecular Weight: 380.533
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116585-41-2.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: C27H28N2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C27H28N2(116585-41-2)
    11. EPA Substance Registry System: C27H28N2(116585-41-2)
  • 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: 116585-41-2(Hazardous Substances Data)

116585-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116585-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,5,8 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 116585-41:
(8*1)+(7*1)+(6*6)+(5*5)+(4*8)+(3*5)+(2*4)+(1*1)=132
132 % 10 = 2
So 116585-41-2 is a valid CAS Registry Number.

116585-41-2Downstream Products

116585-41-2Relevant articles and documents

Intramolecular 2H Group-Transfer (Dyotropic Rearrangements) in Alicyclic and Heterocyclic Bridged-Ring Systems

Mackenzie, K.,Proctor, G.,Woodnutt, D. J.

, p. 5981 - 5994 (2007/10/02)

Examples of alicyclic frameworks containing a cyclohexa-1,3-diene ring as 2H donor held proximate to a variously-substituted acceptor Π-bond are compared for their reactivity in thermal 2H group-transfer reactions.Kinetic analysis reveals marked effects on rearrangement-rate as the acceptor Π-bond substituents are varied.Attempted synthesis of exact structural analogues of these compounds but with a 2,3-diazacyclohexadiene component replacing the cyclohexadiene element usually gives instead products of concomitant 2H group-transfer.These results are compared with the similar but generally slower 2H group-transfer rearrangement of pentacyclic 2-pyrazoline derivatives having relevant critical stereochemical features which result from 1,3 -diarylnitrilimine (4+2)Π adductions with dipolarophiles of the isodrin type.Alkoxy and chlorine substitution of the acceptor Π-bond is rate-retarding for 2H group-transfer in both the alicyclic and heterocyclic representative systems examined, indicating truly pericyclic behaviour.

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