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117568-53-3

1,3,5-triphenylethyl-1,3,5-triazacyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 117568-53-3 Structure

  • Basic information

    1. Product Name: 1,3,5-triphenylethyl-1,3,5-triazacyclohexane
    2. Synonyms: 1,3,5-triphenylethyl-1,3,5-triazacyclohexane
    3. CAS NO:117568-53-3
    4. Molecular Formula:
    5. Molecular Weight: 399.579
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 117568-53-3.mol
    9. Article Data: 2

  • 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: 1,3,5-triphenylethyl-1,3,5-triazacyclohexane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3,5-triphenylethyl-1,3,5-triazacyclohexane(117568-53-3)
    11. EPA Substance Registry System: 1,3,5-triphenylethyl-1,3,5-triazacyclohexane(117568-53-3)

  • 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: 117568-53-3(Hazardous Substances Data)

117568-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117568-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,5,6 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 117568-53:
(8*1)+(7*1)+(6*7)+(5*5)+(4*6)+(3*8)+(2*5)+(1*3)=143
143 % 10 = 3
So 117568-53-3 is a valid CAS Registry Number.

117568-53-3Relevant articles and documents

Role of hydroxyl groups on the aromatic ring in the reactivity and selectivity of the reaction of β -phenylethylamines with non-enolizable aldehydes

Quevedo, Rodolfo,Díaz-Oviedo, Christian,Quevedo-Acosta, Yovanny

, p. 9835 - 9843 (2015)

The influence of hydroxyl groups on the β-phenylethylamine aromatic ring was studied during its reaction with non-enolizable aldehydes. Computational calculations established that the degree of hydroxylation generates differences in the activation pattern

The Synthesis of 2-Arylmethyltetrahydroisoquinolines from Bis(Aminol) Ethers Involving Two Iminium Salt Intermediates

Heaney, Harry,Papageorgiou, George,Wilkins, Robert F.

, p. 10737 - 10750 (2007/10/02)

The bis(aminol) ether derived from 3,4-dimethoxy-β-phenylethylamine, methanol, and formaldehyde reacts with trichloromethylsilane to afford an equilibrium mixture of N-chloromethyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline and its related iminium chloride.Interaction with electron rich aromatic compounds afford good yields of N-arylmethyl derivatives, including sendaverine methyl ether.Reactions of the bis(amino) ether in the presence of the aromatic substrate allows the formation of the N-arylmethyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline derivatives in a one pot reaction.

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