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CAS

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1372129-04-8

(2R,5E)-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-6-iodo-N,2-dimethylhex-5-enamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1372129-04-8 Structure

  • Basic information

    1. Product Name: (2R,5E)-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-6-iodo-N,2-dimethylhex-5-enamide
    2. Synonyms: (2R,5E)-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-6-iodo-N,2-dimethylhex-5-enamide
    3. CAS NO:1372129-04-8
    4. Molecular Formula:
    5. Molecular Weight: 401.288
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1372129-04-8.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: (2R,5E)-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-6-iodo-N,2-dimethylhex-5-enamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,5E)-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-6-iodo-N,2-dimethylhex-5-enamide(1372129-04-8)
    11. EPA Substance Registry System: (2R,5E)-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-6-iodo-N,2-dimethylhex-5-enamide(1372129-04-8)

  • 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: 1372129-04-8(Hazardous Substances Data)

1372129-04-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1372129-04-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,2,1,2 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1372129-04:
(9*1)+(8*3)+(7*7)+(6*2)+(5*1)+(4*2)+(3*9)+(2*0)+(1*4)=138
138 % 10 = 8
So 1372129-04-8 is a valid CAS Registry Number.

1372129-04-8Downstream Products

1372129-04-8Relevant articles and documents

Asymmetric total synthesis and absolute stereochemistry of the neuroactive marine macrolide palmyrolide A

Tello-Aburto, Rodolfo,Johnson, Emily M.,Valdez, Cheyenne K.,Maio, William A.

, p. 2150 - 2153 (2012)

The first asymmetric total synthesis and determination of the absolute configuration for the neuroactive marine macrolide palmyrolide A is described. The highlight of the synthesis is macrocyclization via trans-enamide formation catalyzed by copper(I) iodide and cesium carbonate. Comparison with the authentic spectral data confirms the synthesis of (+)-ent-palmyrolide A.

Evolution of a protecting-group-free total synthesis: Studies en route to the neuroactive marine macrolide (-)-palmyrolide A

Tello-Aburto, Rodolfo,Newar, Tara D.,Maio, William A.

experimental part, p. 6271 - 6289 (2012/09/22)

A full account of our synthetic work toward the first total synthesis of the neuroactive marine macrolide (-)-palmyrolide A is described. Our first-generation approach aimed to unlock the unknown C(5)-C(7) stereochemical relationship via the synthesis of

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