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(R)-1,1’-binaphthl-2,2’-dicarbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 121314-72-5 Structure
  • Basic information

    1. Product Name: (R)-1,1’-binaphthl-2,2’-dicarbaldehyde
    2. Synonyms: (R)-1,1’-binaphthl-2,2’-dicarbaldehyde
    3. CAS NO:121314-72-5
    4. Molecular Formula:
    5. Molecular Weight: 310.352
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121314-72-5.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: (R)-1,1’-binaphthl-2,2’-dicarbaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-1,1’-binaphthl-2,2’-dicarbaldehyde(121314-72-5)
    11. EPA Substance Registry System: (R)-1,1’-binaphthl-2,2’-dicarbaldehyde(121314-72-5)
  • 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: 121314-72-5(Hazardous Substances Data)

121314-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121314-72-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,3,1 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 121314-72:
(8*1)+(7*2)+(6*1)+(5*3)+(4*1)+(3*4)+(2*7)+(1*2)=75
75 % 10 = 5
So 121314-72-5 is a valid CAS Registry Number.

121314-72-5Relevant articles and documents

Mild synthesis of enantiomerically pure imidazo-[1,2-a]azepines mediated by Yb(OTf)3

Annunziata, Rita,Benaglia, Maurizio,Raimondi, Laura

, p. 10357 - 10363 (2001)

The reaction of various chiral 2,2′-diaryldialdehydes with achiral and chiral 1,2-diamines in the presence of Lewis acids to give imidazo[1,2-a]azepines was investigated. Best results were achieved with Yb(OTf)3; the reaction outcome is strongly dependent upon the geometric features of both reactants. Kinetic resolution of rac-2,2′-dinaphthyldialdehyde with (R,R)-1,2-diphenyl-1,2-diamminoethane (up to 92% e.e.) was achieved.

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