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1569807-15-3

(11bR)-8,9,10,11,12,13,14,15-Octahydro-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. is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (11bR)-2,6-di([1,1':3',1''-terphenyl]-5'-yl)-4-hydroxy-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide

    Cas No: 1569807-15-3

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  • (11bR)?-8,?9,?10,?11,?12,?13,?14,?15-?Octahydro-?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

    Cas No: 1569807-15-3

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  • (11bR)-8,9,10,11,12,13,14,15-Octahydro-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.

    Cas No: 1569807-15-3

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  • (11bR)-8,9,10,11,12,13,14,15-Octahydro-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: 1569807-15-3

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  • 1569807-15-3 Structure

  • Basic information

    1. Product Name: (11bR)-8,9,10,11,12,13,14,15-Octahydro-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.
    2. Synonyms: (11bR)-8,9,10,11,12,13,14,15-Octahydro-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.;R-3,3'-Bis[1,1':3',1''-terphenyl]-5,5',6,6',7,7',8,8'-Octahydro-1,1'-bi-2-naphthyl phosphate
    3. CAS NO:1569807-15-3
    4. Molecular Formula: C56H45O5P
    5. Molecular Weight: 828.927261
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1569807-15-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.34±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 1.14±0.20(Predicted)
    10. CAS DataBase Reference: (11bR)-8,9,10,11,12,13,14,15-Octahydro-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.(CAS DataBase Reference)
    11. NIST Chemistry Reference: (11bR)-8,9,10,11,12,13,14,15-Octahydro-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.(1569807-15-3)
    12. EPA Substance Registry System: (11bR)-8,9,10,11,12,13,14,15-Octahydro-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.(1569807-15-3)

  • 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: 1569807-15-3(Hazardous Substances Data)

1569807-15-3 Usage

Uses

Used in Pharmaceutical Research:
Used in Agrochemical Research:
Used in Materials Science Research:

Check Digit Verification of cas no

The CAS Registry Mumber 1569807-15-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,8,0 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1569807-15:
(9*1)+(8*5)+(7*6)+(6*9)+(5*8)+(4*0)+(3*7)+(2*1)+(1*5)=213
213 % 10 = 3
So 1569807-15-3 is a valid CAS Registry Number.

1569807-15-3Upstream product

1569807-15-3Downstream Products

1569807-15-3Relevant articles and documents

N-Boc-aminals as easily accessible precursors for less accessible N-Boc-imines: Facile synthesis of optically active propargylamine derivatives using Mannich-type reactions

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

, p. 3687 - 3700 (2016/06/06)

We developed a facile and practical synthesis of N-Boc-aminals, which can be used as precursors for less accessible N-Boc-imines. Aminals were obtained via simple dehydration condensation reactions of t-butyl carbamate (BocNH2) and various aldehydes in acetic anhydride, followed by filtration and washing with hexane. The obtained N-Boc-alkynylaminals could be successfully applied in enantioselective Mannich-type reactions, catalyzed by chiral phosphoric acids, to afford optically active propargylamine derivatives.

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

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