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154520-14-6

(2S)-(1'S,2'R,4'R)-10'-(dicyclohexylsulfamoyl)isobornyl-2-cyano-2-ethyl-4-pentenoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 154520-14-6 Structure

  • Basic information

    1. Product Name: (2S)-(1'S,2'R,4'R)-10'-(dicyclohexylsulfamoyl)isobornyl-2-cyano-2-ethyl-4-pentenoate
    2. Synonyms: (2S)-(1'S,2'R,4'R)-10'-(dicyclohexylsulfamoyl)isobornyl-2-cyano-2-ethyl-4-pentenoate
    3. CAS NO:154520-14-6
    4. Molecular Formula:
    5. Molecular Weight: 532.788
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 154520-14-6.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: (2S)-(1'S,2'R,4'R)-10'-(dicyclohexylsulfamoyl)isobornyl-2-cyano-2-ethyl-4-pentenoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S)-(1'S,2'R,4'R)-10'-(dicyclohexylsulfamoyl)isobornyl-2-cyano-2-ethyl-4-pentenoate(154520-14-6)
    11. EPA Substance Registry System: (2S)-(1'S,2'R,4'R)-10'-(dicyclohexylsulfamoyl)isobornyl-2-cyano-2-ethyl-4-pentenoate(154520-14-6)

  • 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: 154520-14-6(Hazardous Substances Data)

154520-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154520-14-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,5,2 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 154520-14:
(8*1)+(7*5)+(6*4)+(5*5)+(4*2)+(3*0)+(2*1)+(1*4)=106
106 % 10 = 6
So 154520-14-6 is a valid CAS Registry Number.

154520-14-6Relevant articles and documents

Lipopeptaibol metabolites of tolypocladium geodes: Total synthesis, preferred conformation, and membrane activity

Rainaldi, Mario,Moretto, Alessandro,Peggion, Cristina,Formaggio, Fernando,Mammi, Stefano,Peggion, Evaristo,Galvez, Jose Antonio,Diaz-de-Villegas, Maria Dolores,Cativiela, Carlos,Toniolo, Claudio

, p. 3567 - 3576 (2007/10/03)

We have synthesized by solution methods and characterized the lipopeptaibol metabolite LP237-F8 extracted from the fungus Tolypocladium geodes and five selected analogues with the Etn → Aib or Etn → Nva replacement at position 8 and/or a triple Gln → Glu(OMe) replacement at positions 5, 6, and 9 (Etn = Cα-ethylnorvaline, Aib = α-aminoisobutyric acid, Nva = norvaline). Conformation analysis, performed by FT-IR absorption, NMR, and CD techniques, strongly supports the view that the six terminally blocked decapeptides are highly helical in solution. Helix topology and amphiphilic character are responsible for their remarkable membrane activity. At position 8 the combination of high hydrophobicity and Ca tetrasubstitution, as in the Etn-containing LP237-F8 metabolite, has a positive effect on membrane interaction.

Asymmetric Synthesis of β-Lactams. Highly Diastereoselective Alkylation of Chiral 2-Cyano Esters

Cativiela, Carlos,Diaz-de-Villegas, Maria D.,Galvez, Jose A.

, p. 2497 - 2505 (2007/10/02)

Enolates derived from 10-(dicyclohexylsulfamoyl)isobornyl 2-substituted-2-cyanoacetates were alkylated with very good yield and high diastereoselectivity.The reduction of the resulting reaction products and subsequent cyclization of the β-amino acids led

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