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1416470-39-7

(E,S)-3-(4-chlorophenyl)-1-phenylallyl 4-nitrobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1416470-39-7 Structure

  • Basic information

    1. Product Name: (E,S)-3-(4-chlorophenyl)-1-phenylallyl 4-nitrobenzoate
    2. Synonyms:
    3. CAS NO:1416470-39-7
    4. Molecular Formula:
    5. Molecular Weight: 393.826
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1416470-39-7.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: (E,S)-3-(4-chlorophenyl)-1-phenylallyl 4-nitrobenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E,S)-3-(4-chlorophenyl)-1-phenylallyl 4-nitrobenzoate(1416470-39-7)
    11. EPA Substance Registry System: (E,S)-3-(4-chlorophenyl)-1-phenylallyl 4-nitrobenzoate(1416470-39-7)

  • 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: 1416470-39-7(Hazardous Substances Data)

1416470-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1416470-39-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,6,4,7 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1416470-39:
(9*1)+(8*4)+(7*1)+(6*6)+(5*4)+(4*7)+(3*0)+(2*3)+(1*9)=147
147 % 10 = 7
So 1416470-39-7 is a valid CAS Registry Number.

1416470-39-7Downstream Products

1416470-39-7Relevant articles and documents

Ion pair dynamics: Solvolyses of chiral 1,3-diarylallyl carboxylates as a case study

Troshin, Konstantin,Mayr, Herbert

, p. 252 - 265 (2013)

Chiral ion pairs play a key role in modern enantioselective synthesis, though little is known about their properties. We have now used the special features of unsymmetrically substituted allyl derivatives to obtain unprecedented insight into ion pair dynamics. By employing chiral high-performance liquid chromatography, it was possible to follow the time-dependent concentrations of all four isomeric esters (two regioisomeric pairs of enantiomers) and all four isomeric alcohols generated during the hydrolysis of enantiopure 1-(4-chlorophenyl)-3-phenylallyl and 3-(4-chlorophenyl)-1-phenylallyl 4-nitrobenzoates. Combination of these results with the directly measured rate constant for the reaction of the laser-flash photolytically generated 1-(4-chlorophenyl)-3-phenylallyl cation with water provided a complete mechanistic scheme for allyl carboxylate solvolysis. It is demonstrated that solvolysis and internal return can be explained by the same intermediates. The correlation equation log k = sN(N + E) was used to elucidate the variable importance of external and internal return in the solvolysis reactions. This information will be crucial for the interpretation of the ultrafast dynamics of ion pairs generated by femtosecond laser pulses.

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