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1,2-Diphenyl-dodecan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127464-94-2 Structure
  • Basic information

    1. Product Name: 1,2-Diphenyl-dodecan
    2. Synonyms: 1,2-Diphenyl-dodecan
    3. CAS NO:127464-94-2
    4. Molecular Formula:
    5. Molecular Weight: 322.534
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127464-94-2.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: 1,2-Diphenyl-dodecan(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Diphenyl-dodecan(127464-94-2)
    11. EPA Substance Registry System: 1,2-Diphenyl-dodecan(127464-94-2)
  • 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: 127464-94-2(Hazardous Substances Data)

127464-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127464-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,4,6 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 127464-94:
(8*1)+(7*2)+(6*7)+(5*4)+(4*6)+(3*4)+(2*9)+(1*4)=142
142 % 10 = 2
So 127464-94-2 is a valid CAS Registry Number.

127464-94-2Downstream Products

127464-94-2Relevant articles and documents

Modification of Photochemical Reactivity by Cyclodextrin Complexation: A Remarkable Effect on the Photobehavior of α-Alkyldibenzyl Ketones

Nageshwer Rao, B.,Syamala, M. S.,Turro, N. J.,Ramamurthy, V.

, p. 5517 - 5521 (1987)

The Norrish type I and type II reactions of cyclodextrin-included α-alkyldibenzyl ketones have been investigated in the aqueous solution and in the solid state.The photolysis of solid cyclodextrin complexes led to a single product, diphenylethane (AB), and that of complexes in the aqueous solution resulted in a product arising from the rerrangement of α-alkyldibenzyl ketones.Conformational and super-cage effects are proposed to be responsible for the dramatic alteration observed in the above photobehavior.The difference in the product distribution between solid and solution complexes is attributed to the differences in the restriction imposed by the host on the translational motions of the geminate radical pairs.

Norrish Type I and Type II Reactions of Ketones as Photochemical Probes of the Interior of Zeolites

Ramamurthy, V.,Corbin, D. R.,Eaton, D. F.

, p. 5269 - 5278 (2007/10/02)

The Norrish type I and type II reactions of alkylbenzoin ethers, alkyldeoxybenzoins and α-alkyldibenzyl ketones included within the microporous structures of zeolites X and Y have been investigated.Product distributions varied significantly from that observed in benzene.In addition, it differed between various alkali-metal cation-exchanged samples.These variations are interpreted to result from the restriction offered by the zeolite micropores on the motions of the adsorbed organic molecule.Although this study is restricted to ketones, the knowledge gained is expected to be of general value.

MODIFICATION OF PHOTOCHEMICAL REACTIVITY BY ZEOLITES: ROLE OF CATIONS IN CONTROLLING THE BEHAVIOR OF RADICALS GENERATED WITHIN FAUJASITES.

Ramamurthy, V.,Corbin, D. R.,Eaton, D. F.,Turro, N. J.

, p. 5833 - 5836 (2007/10/02)

α-Alkyldibenzylketones included in cation exchanged faujasite type zeolites show photobehavior different from that in isotropic organic solvents.Rearrangement and disproportionation which do not contribute in solution are the major processes within the cavities of faujasites.Cation size plays a major role in controlling the pathway pursued by the primary and the secondary radical pair.

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