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1214919-09-1

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

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  • 1214919-09-1 Structure

  • Basic information

    1. Product Name: (-)-donaxaridine
    2. Synonyms: (-)-donaxaridine
    3. CAS NO:1214919-09-1
    4. Molecular Formula:
    5. Molecular Weight: 206.244
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1214919-09-1.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: (-)-donaxaridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-donaxaridine(1214919-09-1)
    11. EPA Substance Registry System: (-)-donaxaridine(1214919-09-1)

  • 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: 1214919-09-1(Hazardous Substances Data)

1214919-09-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1214919-09-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,9,1 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1214919-09:
(9*1)+(8*2)+(7*1)+(6*4)+(5*9)+(4*1)+(3*9)+(2*0)+(1*9)=141
141 % 10 = 1
So 1214919-09-1 is a valid CAS Registry Number.

1214919-09-1Downstream Products

1214919-09-1Relevant articles and documents

Highly enantioselective aldol reaction of acetaldehyde and isatins only with 4-hydroxydiarylprolinol as catalyst: concise stereoselective synthesis of (R)-convolutamydines B and E, (-)-donaxaridine and (R)-chimonamidine

Chen, Wen-Bing,Du, Xi-Lin,Cun, Lin-Feng,Zhang, Xiao-Mei,Yuan, Wei-Cheng

, p. 1441 - 1446 (2010)

A highly enantioselective aldol reaction of acetaldehyde and a wide scope of isatins has been presented only using readily available 4-hydroxydiarylprolinol as catalyst, affording various desired 3-substituted 3-hydroxyindolin-2-one adducts with moderate to high yield (up to 95%) and good enantioselectivities (up to 98% ee). This method not only represents an example of concise stereoselective synthesis of enantiopure (R)-convolutamydines B and E, but also firstly exhibits expedient asymmetric synthesis optically active (-)-donaxaridine and (R)-chimonamidine.

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