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CAS

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1448179-04-1

(4S,5S)-5-cyano-1-(methoxycarbonylmethyl)-4-phenylmethylimidazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1448179-04-1 Structure

  • Basic information

    1. Product Name: (4S,5S)-5-cyano-1-(methoxycarbonylmethyl)-4-phenylmethylimidazolidin-2-one
    2. Synonyms:
    3. CAS NO:1448179-04-1
    4. Molecular Formula:
    5. Molecular Weight: 273.291
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1448179-04-1.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: (4S,5S)-5-cyano-1-(methoxycarbonylmethyl)-4-phenylmethylimidazolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5S)-5-cyano-1-(methoxycarbonylmethyl)-4-phenylmethylimidazolidin-2-one(1448179-04-1)
    11. EPA Substance Registry System: (4S,5S)-5-cyano-1-(methoxycarbonylmethyl)-4-phenylmethylimidazolidin-2-one(1448179-04-1)

  • 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: 1448179-04-1(Hazardous Substances Data)

1448179-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1448179-04-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,1,7 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1448179-04:
(9*1)+(8*4)+(7*4)+(6*8)+(5*1)+(4*7)+(3*9)+(2*0)+(1*4)=181
181 % 10 = 1
So 1448179-04-1 is a valid CAS Registry Number.

1448179-04-1Downstream Products

1448179-04-1Relevant articles and documents

Synthesis and regioselective functionalization of piperazin-2-ones based on Phe-Gly pseudodipeptides

Valdivielso, Angel M.,Ventosa-Andres, Pilar,Garcia-Lopez, M. Teresa,Herranz, Rosario,Gutierrez-Rodriguez, Marta

, p. 155 - 161 (2013/02/26)

The synthesis of 1,4-unsubstituted piperazin-2-ones by one-pot reductive cyclization of PheΨ[CH(CN)NH]Gly pseudodipeptides is described. Studies on the reactivity of the piperazin-2-one ring showed a higher reactivity at the N4 position than at the N1 position. The stepwise regioselective functionalization of piperazin-2-one derivatives showed great potential for molecular diversity generation. An easy methodology for the synthesis of the piperazin-2-ones by one-pot reductive cyclization of PheΨ[CH(CN)NH]Gly pseudodipeptides is described. Study of the reactivity of the piperazin-2-one ring has shown that regioselective functionalization at the N1 and N4 positions is possible, and hence great potential for molecular diversity generation Copyright

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