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1446558-34-4

ethyl (1S,2S,3R,4R)-3-benzamidobicyclo[2.2.1]hept-5-ene-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • ethyl (1S,2S,3R,4R)-3-benzamidobicyclo[2.2.1]hept-5-ene-2-carboxylate

    Cas No: 1446558-34-4

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  • 1446558-34-4 Structure

  • Basic information

    1. Product Name: ethyl (1S,2S,3R,4R)-3-benzamidobicyclo[2.2.1]hept-5-ene-2-carboxylate
    2. Synonyms: ethyl (1S,2S,3R,4R)-3-benzamidobicyclo[2.2.1]hept-5-ene-2-carboxylate
    3. CAS NO:1446558-34-4
    4. Molecular Formula:
    5. Molecular Weight: 285.343
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446558-34-4.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: ethyl (1S,2S,3R,4R)-3-benzamidobicyclo[2.2.1]hept-5-ene-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl (1S,2S,3R,4R)-3-benzamidobicyclo[2.2.1]hept-5-ene-2-carboxylate(1446558-34-4)
    11. EPA Substance Registry System: ethyl (1S,2S,3R,4R)-3-benzamidobicyclo[2.2.1]hept-5-ene-2-carboxylate(1446558-34-4)

  • 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: 1446558-34-4(Hazardous Substances Data)

1446558-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446558-34-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,5,5 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1446558-34:
(9*1)+(8*4)+(7*4)+(6*6)+(5*5)+(4*5)+(3*8)+(2*3)+(1*4)=184
184 % 10 = 4
So 1446558-34-4 is a valid CAS Registry Number.

1446558-34-4Relevant articles and documents

Stereocontrolled one-step synthesis of difunctionalised cispentacin derivatives through ring-opening metathesis of norbornene β-amino acids

Kiss, Lornd,Kardos, Mrton,Forr, Eniko,Fül?p, Ferenc

, p. 1283 - 1289 (2015)

Through the ring-opening metathesis of norbornene or oxanorbornene β-amino acids with ethylene in the presence of certain Ru catalysts, a facile and convenient stereocontrolled one-step method was devised for the preparation of divinylated cispentacins an

A new access route to functionalized cispentacins from norbornene β-amino acids

Kiss, Loránd,Cherepanova, Maria,Forró, Eniko,Fül?p, Ferenc

, p. 2102 - 2107 (2013/03/28)

An efficient and simple new stereocontrolled access route to novel disubstituted cispentacin derivatives with multiple stereogenic centers from norbornene β-lactam has been developed. The synthesis involves olefinic bond functionalization by dihydroxylation followed by oxidative ring cleavage and transformation of the dialdehyde intermediate through a Wittig reaction. Copyright

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