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R- 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 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 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

    Cas No: 361342-55-4

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  • R- 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

    Cas No: 361342-55-4

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  • (11bR)-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: 361342-55-4

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  • 361342-55-4 Structure
  • Basic information

    1. Product Name: R- 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
    2. Synonyms: R- 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;(R)-3,3'-Bis(3,5-diphenyl)phenyl-1,1'-binaphthyl-2,2'-diyl Hydrogen Phosphate;(11bR)-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;(11bR)-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.
    3. CAS NO:361342-55-4
    4. Molecular Formula: C56H37O4P
    5. Molecular Weight: 804.864341
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 361342-55-4.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: R- 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(CAS DataBase Reference)
    11. NIST Chemistry Reference: R- 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(361342-55-4)
    12. EPA Substance Registry System: R- 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(361342-55-4)
  • 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: 361342-55-4(Hazardous Substances Data)

361342-55-4 Usage

Uses

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Used in Material Science:
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Check Digit Verification of cas no

The CAS Registry Mumber 361342-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,1,3,4 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 361342-55:
(8*3)+(7*6)+(6*1)+(5*3)+(4*4)+(3*2)+(2*5)+(1*5)=124
124 % 10 = 4
So 361342-55-4 is a valid CAS Registry Number.

361342-55-4Upstream product

361342-55-4Downstream Products

361342-55-4Relevant 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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