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59060-56-9

Triphenyl-((2E,4E,6E)-3,7,11-trimethyl-dodeca-2,4,6,10-tetraenyl)-phosphonium; bromide is a complex organic compound with the chemical formula C33H38BrP. It is a phosphonium salt, which consists of a phosphonium cation (triphenyl-((2E,4E,6E)-3,7,11-trimethyl-dodeca-2,4,6,10-tetraenyl)-phosphonium) and a bromide anion. The compound features a conjugated diene system with three methyl groups at positions 3, 7, and 11, and a phosphorus atom bonded to three phenyl rings. triphenyl-((2E,4E,6E)-3,7,11-trimethyl-dodeca-2,4,6,10-tetraenyl)-phosphonium; bromide is likely to be used in organic synthesis, particularly in reactions involving phosphorus-containing compounds, and may have applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals.

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  • 59060-56-9 Structure

  • Basic information

    1. Product Name: triphenyl-((2E,4E,6E)-3,7,11-trimethyl-dodeca-2,4,6,10-tetraenyl)-phosphonium; bromide
    2. Synonyms:
    3. CAS NO:59060-56-9
    4. Molecular Formula:
    5. Molecular Weight: 545.542
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 59060-56-9.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: triphenyl-((2E,4E,6E)-3,7,11-trimethyl-dodeca-2,4,6,10-tetraenyl)-phosphonium; bromide(CAS DataBase Reference)
    10. NIST Chemistry Reference: triphenyl-((2E,4E,6E)-3,7,11-trimethyl-dodeca-2,4,6,10-tetraenyl)-phosphonium; bromide(59060-56-9)
    11. EPA Substance Registry System: triphenyl-((2E,4E,6E)-3,7,11-trimethyl-dodeca-2,4,6,10-tetraenyl)-phosphonium; bromide(59060-56-9)

  • 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: 59060-56-9(Hazardous Substances Data)

59060-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59060-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,6 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59060-56:
(7*5)+(6*9)+(5*0)+(4*6)+(3*0)+(2*5)+(1*6)=129
129 % 10 = 9
So 59060-56-9 is a valid CAS Registry Number.

59060-56-9Relevant articles and documents

43. Das Carotinoidspectrum der Hagebutten von Rosa pomifera: Nachweis von (5Z)-Neurosporin; Synthese von (3R,15Z)-Rubixanthin

Maerki-Fischer, Edith,Marti, Urs,Buchecker, Richard,Eugsten, Conrad Hans

, p. 494 - 513 (1983)

Extensive chromatographic separations of the mixture of carotenoids from ripe hips of R. pomifera have led to the identification of 43 individual compounds, namely (Scheme 2): (15Z)-phytoene (1), (15Z)-phytofluene (2), all-(E)-phytofluene (2a), ξ-carotene (3), two mono-(Z)-ξ-carotenes (3a and 3b), (6R)-ε,ψ-carotene (4), a mono-(Z)-ε,ψ-carotene (4a), β,ψ-carotene (5), a mono-(Z)-β,ψ-carotene (5a), neurosporene (6), (5Z)-neurodporene (6a), a mono-(Z)-neurosporene (6b), lycopene (7), five (Z)-lycopenes (7a-7e), β,β-carotene (8), two mono-(Z)-β,β-carotenes (probably (9Z)-β;β-carotene (8a) and (13Z)-β,β-carotene (8b)), β-cryptoxanthin (9), three (Z)-β-cryptoxanthins (9a-9c), rubixanthin (10), (5'Z)-rubixanthin (=gazaniaxanthin; 10a), (9'Z)-rubixanthin (10b), (13'Z)- and (13Z)-rubixanthin (10c and 10d, resp.), (5'Z, 13'Z)- or (5'Z,13Z)-rubixanthin (10e), lutein (11), zeaxanthin (12), (13Z)-zeaxanthin (12b), a mono-(Z)-zeaxanthin (probably (9Z)-zeaxanthin (12a)), (8R)-mutatoxanthin (13), (8S)-mutatoxanthin (14), neoxanthin (15), (8'R)-neochrome (16), (8'S)-neochrome (17), a tetrahydroxycarotenoid (18?), a tetrahydroxy-epoxy-carotenoid (19?), and a trihydroxycarotenoid of unknown structure.Rubixanthin (10) and (5'Z)-rubixanthin (10a) can be easily distinguished by HPLC. separation and CD. spectra at low temperature.The synthesis of (3R, 15Z)-rubixanthin (29) is described.The isolation of (5Z)-neurosporene (6a) supports the hypothesis that the ε-end group arises by enzymatic cyclization of precursors having a (5Z)- or (5'Z)-configuration.

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