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CAS

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1446558-44-6

ethyl (1S,2R,3S,5R)-2-benzamido-3,5-di(3’-oxobutyl)cyclopentanecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446558-44-6 Structure

  • Basic information

    1. Product Name: ethyl (1S,2R,3S,5R)-2-benzamido-3,5-di(3’-oxobutyl)cyclopentanecarboxylate
    2. Synonyms: ethyl (1S,2R,3S,5R)-2-benzamido-3,5-di(3’-oxobutyl)cyclopentanecarboxylate
    3. CAS NO:1446558-44-6
    4. Molecular Formula:
    5. Molecular Weight: 401.503
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446558-44-6.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,2R,3S,5R)-2-benzamido-3,5-di(3’-oxobutyl)cyclopentanecarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl (1S,2R,3S,5R)-2-benzamido-3,5-di(3’-oxobutyl)cyclopentanecarboxylate(1446558-44-6)
    11. EPA Substance Registry System: ethyl (1S,2R,3S,5R)-2-benzamido-3,5-di(3’-oxobutyl)cyclopentanecarboxylate(1446558-44-6)

  • 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: 1446558-44-6(Hazardous Substances Data)

1446558-44-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446558-44-6 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, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1446558-44:
(9*1)+(8*4)+(7*4)+(6*6)+(5*5)+(4*5)+(3*8)+(2*4)+(1*4)=186
186 % 10 = 6
So 1446558-44-6 is a valid CAS Registry Number.

1446558-44-6Downstream Products

1446558-44-6Relevant articles and documents

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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