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134420-09-0

N-benzyl-1-formamidocyclopentane-1-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134420-09-0 Structure

  • Basic information

    1. Product Name: N-benzyl-1-formamidocyclopentane-1-carboxamide
    2. Synonyms: N-benzyl-1-formamidocyclopentane-1-carboxamide
    3. CAS NO:134420-09-0
    4. Molecular Formula:
    5. Molecular Weight: 246.309
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134420-09-0.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: N-benzyl-1-formamidocyclopentane-1-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzyl-1-formamidocyclopentane-1-carboxamide(134420-09-0)
    11. EPA Substance Registry System: N-benzyl-1-formamidocyclopentane-1-carboxamide(134420-09-0)

  • 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: 134420-09-0(Hazardous Substances Data)

134420-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134420-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,4,2 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 134420-09:
(8*1)+(7*3)+(6*4)+(5*4)+(4*2)+(3*0)+(2*0)+(1*9)=90
90 % 10 = 0
So 134420-09-0 is a valid CAS Registry Number.

134420-09-0Relevant articles and documents

Formation of Imidazolones by Ring Closure of α-Isocyanoamides: Exploring New Reactivities

Baudequin, Christine,Bischoff, Laurent,Frippiat, Steven,Hoarau, Christophe,Leterrier, Claire

, p. 1211 - 1215 (2020/07/20)

Base-mediated ring closure of α,α-disubstituted α-isocyanoamides with further electrophilic trapping has previously been explored, but with limited applications. In this work, we wished to unravel the reactivities of these compounds and, in particular, to allow palladium-catalyzed coupling at the C2 position.

Transition-Metal-Free Synthesis of 2-Arylimidazolones via Cascade Reaction between Arynes and α,α′-Disubstituted α-Isocyanoacetamides

Gesù, Alessandro,Pozzoli, Claudio,Torre, Enza,Aprile, Silvio,Pirali, Tracey

supporting information, p. 1992 - 1995 (2016/06/01)

The reaction between arynes and secondary α,α′-disubstituted α-isocyanoacetamides was developed to access 2-arylimidazolones of structural diversity and complexity in a straightforward manner.

Pd-Catalyzed direct C-H functionalization of imidazolones with aryl- and alkenyl halides

Muselli, Mickal,Baudequin, Christine,Hoarau, Christophe,Bischoff, Laurent

supporting information, p. 745 - 748 (2015/01/09)

Direct C-H arylation and alkenylation of 4,4′-dialkylimidazolones with a broad range of halides under palladium and copper catalysis have been developed. This methodology is applied to the preparation of recently discovered fatty acid synthetase (FAS) inhibitors. This journal is

Studies on Isocyanides and Related Compounds. - Synthesis and Cyclization of N-Substituted 1-Isocyano-1-cycloalkanecarboxamides

Bossio, Ricardo,Marcaccini, Stefano,Paoli, Paola,Papaleo, Sandro,,Pepino, Roberto,Polo, Cecilia

, p. 843 - 849 (2007/10/02)

The Ugi four-component condensation between cycloalkanones, isocyanides, and ammonium formate affords N-substituted 1-formylamino-1-cycloalkanecarboxamides 1 which are dehydrated to give the corresponding isocyanides 2.Compounds 2 are cyclized with arylsu

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