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C11H9Cl3N2O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1374003-08-3 Structure
  • Basic information

    1. Product Name: C11H9Cl3N2O4
    2. Synonyms:
    3. CAS NO:1374003-08-3
    4. Molecular Formula:
    5. Molecular Weight: 339.562
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1374003-08-3.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: C11H9Cl3N2O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H9Cl3N2O4(1374003-08-3)
    11. EPA Substance Registry System: C11H9Cl3N2O4(1374003-08-3)
  • 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: 1374003-08-3(Hazardous Substances Data)

1374003-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374003-08-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,0,0 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1374003-08:
(9*1)+(8*3)+(7*7)+(6*4)+(5*0)+(4*0)+(3*3)+(2*0)+(1*8)=123
123 % 10 = 3
So 1374003-08-3 is a valid CAS Registry Number.

1374003-08-3Downstream Products

1374003-08-3Relevant articles and documents

Copper bis(oxazolines) as catalysts for stereoselective aziridination of styrenes with N-tosyloxycarbamates

Lebel, Hélne,Parmentier, Micha?l,Leogane, Olivier,Ross, Karen,Spitz, Cédric

scheme or table, p. 3396 - 3409 (2012/06/15)

A Cu(I)-catalyzed asymmetric aziridination of styrenes with a chiral N-tosyloxycarbamate has been developed. Double stereodifferentiation was observed and both the N-tosyloxycarbamate substituent and the bis(oxazoline) ligand have a significant effect on the yields and diastereoselectivities. The best results for the aziridination were obtained with electron-deficient styrenes. Subsequent ring-opening reactions of styrene-derived aziridines at the benzylic position were observed with various oxygen and nitrogen nucleophiles under Lewis acid catalysis affording the corresponding products with complete inversion of stereochemistry. The strategy was used to synthesize the β-blocker, (R)-nifenalol.

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