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(1-METHYL-1H-INDOL-3-YL)(PIPERIDINO)METHANONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 207619-48-5 Structure
  • Basic information

    1. Product Name: (1-METHYL-1H-INDOL-3-YL)(PIPERIDINO)METHANONE
    2. Synonyms: (1-METHYL-1H-INDOL-3-YL)(PIPERIDINO)METHANONE;1-methyl-3-(piperidine-1-carbonyl)-1H-indole
    3. CAS NO:207619-48-5
    4. Molecular Formula: C15H18N2O
    5. Molecular Weight: 242.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 207619-48-5.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-METHYL-1H-INDOL-3-YL)(PIPERIDINO)METHANONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1-METHYL-1H-INDOL-3-YL)(PIPERIDINO)METHANONE(207619-48-5)
    11. EPA Substance Registry System: (1-METHYL-1H-INDOL-3-YL)(PIPERIDINO)METHANONE(207619-48-5)
  • 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: 207619-48-5(Hazardous Substances Data)

207619-48-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 207619-48-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,6,1 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 207619-48:
(8*2)+(7*0)+(6*7)+(5*6)+(4*1)+(3*9)+(2*4)+(1*8)=135
135 % 10 = 5
So 207619-48-5 is a valid CAS Registry Number.

207619-48-5Downstream Products

207619-48-5Relevant articles and documents

A novel radical cyclization of 2-bromoindoles. Synthesis of hexahydropyrrolo[3,4-b]indoles

Gribble,Fraser,Badenock

, p. 805 - 806 (2001)

Hexahydropyrrolo[3,4-b]indoles 6, 10, and 13 are obtained from 2-bromo-3-carboxamides 5, 9, and 12, respectively, by a 1,5-radical translocation process followed by 5-endo-trig cyclization to the indole C-2 position.

Acylative Coupling of Amine and Indole Using Chloroform as a Carbonyl Group

Nishida, Yuika,Takeda, Norihiko,Matsuno, Kenji,Miyata, Okiko,Ueda, Masafumi

, p. 3928 - 3935 (2018/07/31)

Chloroform-mediated acylative coupling of amines with indoles has been developed. When indoles and amines in chloroform were treated with dimethylzinc in the presence of air, the three-component aminocarbonylation reaction proceeded via in-situ generation of phosgene from chloroform and O2 to provide indole-3-carboxamides in a single operation. Application to the synthesis of biologically active compounds and intramolecular acylation are also described.

Synthesis of indole-3-carboxamides via a haloform cleavage reaction of 3-trifluoroacetylindole with lithium dialkylamides

Hassinger, Heidi L.,Soll, Richard M.,Gribble, Gordon W.

, p. 3095 - 3098 (2007/10/03)

Reaction of 3-trifluoroacetylindole (4) with lithium dialkylamides affords the corresponding indole-3-carboxamides (5) in good to excellent yields.

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