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1-(4-Iodo-piperidin-1-yl)-ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1314310-94-5 Structure
  • Basic information

    1. Product Name: 1-(4-Iodo-piperidin-1-yl)-ethanone
    2. Synonyms: 1-(4-Iodo-piperidin-1-yl)-ethanone
    3. CAS NO:1314310-94-5
    4. Molecular Formula: C7H12INO
    5. Molecular Weight: 253.08075
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1314310-94-5.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: 1-(4-Iodo-piperidin-1-yl)-ethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-Iodo-piperidin-1-yl)-ethanone(1314310-94-5)
    11. EPA Substance Registry System: 1-(4-Iodo-piperidin-1-yl)-ethanone(1314310-94-5)
  • 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: 1314310-94-5(Hazardous Substances Data)

1314310-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1314310-94-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,3,1 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1314310-94:
(9*1)+(8*3)+(7*1)+(6*4)+(5*3)+(4*1)+(3*0)+(2*9)+(1*4)=105
105 % 10 = 5
So 1314310-94-5 is a valid CAS Registry Number.

1314310-94-5Downstream Products

1314310-94-5Relevant articles and documents

PROCESS FOR THE PREPARATION OF N-IODOAMIDES

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Paragraph 00230-00231, (2015/05/26)

The present invention provides new stable crystalline N-iodoamides - 1-iodo- 3,5,5-trimethylhydantoin (1-ITMH) and 3-iodo-4,4-dimethyl-2-oxazolidinone (IDMO). The present invention further provides a process for the preparation of organic iodides using N-iodoamides of this invention and recovery of the amide co-products from waste water.

Metal-free efficient, general and facile iododecarboxylation method with biodegradable co-products

Kulbitski, Kseniya,Nisnevich, Gennady,Gandelman, Mark

supporting information; experimental part, p. 1438 - 1442 (2011/07/30)

The development of a novel, efficient and robust method for the general conversion of aliphatic and aromatic carboxylic acids to organic iodides without the use of heavy metals or strong oxidizing agents is reported. Commercially available N-iodoamides were used for both initiation and halogen donation under irradiative conditions. Isolation of the product is extremely simple and the major co-product is removed as a water-soluble biodegradable material. Copyright

PROCESS FOR THE PREPARATION OF IODIDES

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Page/Page column 28-30, (2012/01/05)

This invention is directed to a process for the preparation of high yield alkyl or aryl iodide from its corresponding carboxylic acid using N-iodo amides.

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