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1496637-05-8

(S)-3,3'-Bis(3,5-diphenyl)phenyl-1,1'-binaphthyl-2,2'-diyl Hydrogen Phosphate is a complex chemical compound with a specific molecular structure. It is characterized by its light-emitting and conducting properties, as well as its high thermal stability.
Used in Organic Electronics Industry:
(S)-3,3'-Bis(3,5-diphenyl)phenyl-1,1'-binaphthyl-2,2'-diyl Hydrogen Phosphate is used as a red-emitting material for organic light-emitting diodes (OLEDs) due to its light-emitting properties and high thermal stability.
Used in Photophysics Applications:
(S)-3,3'-Bis(3,5-diphenyl)phenyl-1,1'-binaphthyl-2,2'-diyl Hydrogen Phosphate is used as a component in photophysical applications due to its light-emitting and conducting properties.
Used in Optoelectronic Devices:
(S)-3,3'-Bis(3,5-diphenyl)phenyl-1,1'-binaphthyl-2,2'-diyl Hydrogen Phosphate is used as a material in organic photovoltaics, organic field-effect transistors, and other organic electronics due to its unique molecular structure and performance characteristics.

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  • (S)-4-Oxide-4-hydroxy-2,6-bis([1,1':3',1''-terphenyl]-5'-yl)-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin;1496637-05-8

    Cas No: 1496637-05-8

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  • bis(13-hydroxy-10,16-bis({5-phenyl-[1,1'-biphenyl]-3-yl})-12,14-dioxa-13λ -phosphapentacyclo[13.8.0.02,11.03, .01 ,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaen-13-one)

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  • (11bS)-4-Hydroxy-2,6-bis([1,1':3',1''-terphenyl]-5'-yl)-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin, 98%, (99% ee)

    Cas No: 1496637-05-8

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  • 1496637-05-8 Structure

  • Basic information

    1. Product Name: (S)-3,3'-Bis(3,5-diphenyl)phenyl-1,1'-binaphthyl-2,2'-diyl Hydrogen Phosphate
    2. Synonyms: (S)-3,3'-Bis(3,5-diphenyl)phenyl-1,1'-binaphthyl-2,2'-diyl Hydrogen Phosphate;(11bS)-4-Hydroxy-2,6-bis([1,1':3',1''-terphenyl]-5'-yl)-4- oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin;(11bS)-4-Hydroxy-2,6-bis([1,1':3',1''-terphenyl]-5'-yl)-4- oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin,99%e.e.;(11bS)-4-Hydroxy-2,6-bis([1,1':3',1''-terphenyl]-5'-yl)-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin, 98%, (99% ee)
    3. CAS NO:1496637-05-8
    4. Molecular Formula: C56H37O4P
    5. Molecular Weight: 804.86
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1496637-05-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.38±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: 1.11±0.20(Predicted)
    10. CAS DataBase Reference: (S)-3,3'-Bis(3,5-diphenyl)phenyl-1,1'-binaphthyl-2,2'-diyl Hydrogen Phosphate(CAS DataBase Reference)
    11. NIST Chemistry Reference: (S)-3,3'-Bis(3,5-diphenyl)phenyl-1,1'-binaphthyl-2,2'-diyl Hydrogen Phosphate(1496637-05-8)
    12. EPA Substance Registry System: (S)-3,3'-Bis(3,5-diphenyl)phenyl-1,1'-binaphthyl-2,2'-diyl Hydrogen Phosphate(1496637-05-8)

  • 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: 1496637-05-8(Hazardous Substances Data)

1496637-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1496637-05-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,9,6,6,3 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1496637-05:
(9*1)+(8*4)+(7*9)+(6*6)+(5*6)+(4*3)+(3*7)+(2*0)+(1*5)=208
208 % 10 = 8
So 1496637-05-8 is a valid CAS Registry Number.

1496637-05-8Upstream product

1496637-05-8Downstream Products

1496637-05-8Relevant articles and documents

Acid-catalyzed in situ generation of less accessible or unprecedented N-Boc imines from N-Boc aminals

Kano, Taichi,Yurino, Taiga,Asakawa, Daisuke,Maruoka, Keiji

supporting information, p. 5532 - 5534 (2013/06/27)

Crafty aminals: The in situ generation of hitherto unattainable alkynyl-substituted N-Boc-protected imines was realized by the acid-catalyzed elimination of tert-butyl carbamate from N-Boc aminals. A wide variety of N-Boc imines can be generated, which ca

Organocatalytic asymmetric synthesis of propargylamines with two adjacent stereocenters: Mannich-type reactions of in situ generated C-alkynyl imines with β-keto esters

Kano, Taichi,Yurino, Taiga,Maruoka, Keiji

supporting information, p. 11509 - 11512 (2013/11/06)

Side by side: The title reaction is catalyzed by the chiral Bronsted acid (S)-1, and affords hitherto less accessible chiral propargylamines, having two adjacent stereocenters, in good to excellent diastereo- and enantioselectivities. Boc=tert-butoxycarbonyl. Copyright

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