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13606-96-7

N-(2-pyridinyl)pentanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13606-96-7 Structure

  • Basic information

    1. Product Name: N-(2-pyridinyl)pentanamide
    2. Synonyms: N-(2-pyridinyl)pentanamide
    3. CAS NO:13606-96-7
    4. Molecular Formula: C10H14N2O
    5. Molecular Weight: 178.23096
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13606-96-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(2-pyridinyl)pentanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-pyridinyl)pentanamide(13606-96-7)
    11. EPA Substance Registry System: N-(2-pyridinyl)pentanamide(13606-96-7)

  • 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: 13606-96-7(Hazardous Substances Data)

13606-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13606-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,0 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13606-96:
(7*1)+(6*3)+(5*6)+(4*0)+(3*6)+(2*9)+(1*6)=97
97 % 10 = 7
So 13606-96-7 is a valid CAS Registry Number.

13606-96-7Relevant articles and documents

Lewis Base-Boryl Radicals Enabled the Desulfurizative Reduction and Annulation of Thioamides

Yu, You-Jie,Zhang, Feng-Lian,Cheng, Jie,Hei, Jing-Hao,Deng, Wei-Ting,Wang, Yi-Feng

supporting information, p. 24 - 27 (2018/01/17)

A new protocol for radical transformations of thioamides promoted by Lewis base-boryl radicals is reported. The desulfurizative reduction to access organic amines was enabled utilizing 4-dimethylaminopyridine-BH3 as the boryl radical precursor and PhSH as the polarity reversal catalyst. Alternatively, the chain process for unsaturated thioamides was switched to an annulation reaction using N-heterocyclic carbene-BH3 as the boryl radical precursor and sterically bulky Ph3CSH as the catalyst, allowing for the construction of N-heterocyclic and carbocyclic skeletons.

Toward versatile methods leading to highly functionalized imidazo[1,2-a]pyridines

Basilio-Lopes, Alexandra,De Aquino, Thiago Mendon?a,Mongeot, Alexandre,Bourguignon, Jean-Jacques,Schmitt, Martine

supporting information; experimental part, p. 2583 - 2587 (2012/07/01)

A convenient and general method of preparation of polyfunctionalized imidazo[1,2-a]pyridines is reported. This methodology involves activation of secondary amides leading to the formation of the corresponding amidines 9. Different activating reagents have

An improved amide coupling procedure for the synthesis of N-(pyridin-2-yl)amides

Londregan, Allyn T.,Storer, Gregory,Wooten, Ceshea,Yang, Xiaojing,Warmus, Joseph

supporting information; experimental part, p. 1986 - 1988 (2009/07/05)

Dehydrative amide couplings with 2-pyridylamines suffer from variable yields. A mild and high-yielding synthesis of N-(pyridin-2-yl)amides employing 2-aminopyridine-N-oxides is presented as a solution.

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