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857284-22-1

3-(piperidin-1-ylmethyl)benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 857284-22-1 Structure

  • Basic information

    1. Product Name: 3-(piperidin-1-ylmethyl)benzonitrile
    2. Synonyms: 3-(piperidin-1-ylmethyl)benzonitrile;Benzonitrile, 3-(1-piperidinylmethyl)-
    3. CAS NO:857284-22-1
    4. Molecular Formula: C13H16N2
    5. Molecular Weight: 200.28
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 857284-22-1.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: 3-(piperidin-1-ylmethyl)benzonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(piperidin-1-ylmethyl)benzonitrile(857284-22-1)
    11. EPA Substance Registry System: 3-(piperidin-1-ylmethyl)benzonitrile(857284-22-1)

  • 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: 857284-22-1(Hazardous Substances Data)

857284-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 857284-22-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,2,8 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 857284-22:
(8*8)+(7*5)+(6*7)+(5*2)+(4*8)+(3*4)+(2*2)+(1*2)=201
201 % 10 = 1
So 857284-22-1 is a valid CAS Registry Number.

857284-22-1Downstream Products

857284-22-1Relevant articles and documents

Method for catalyzing hydrodesulfurization of thioamide derivative

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Paragraph 0029-0033, (2021/07/09)

The invention provides a method for catalyzing hydrodesulfurization of a thioamide derivative, which comprises the following steps: sequentially adding a pentacarbonyl manganese bromide catalyst, a reaction substrate thioamide derivative, Lewis acid, a solvent and alkali into a polytetrafluoroethylene lined reaction tube, putting the reaction tube into a high-pressure kettle, introducing hydrogen to carry out catalytic hydrogenation reaction, cooling to room temperature, discharging gas, washing the reaction tube with ethyl acetate, passing through a silica gel small short column, carrying out spin drying, and carrying out column chromatography purification to obtain a target product. The monovalent manganese which is low in toxicity and good in chemical selectivity and biocompatibility is used as the catalyst to catalyze hydrodesulfurization of the thioamide derivative, the substrate range is wide, the yield of amine is high, and the method has high drug synthesis application value.

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