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264619-96-7

N1-benzyl-N10-(pent-4-ynoyl)tryptamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 264619-96-7 Structure

  • Basic information

    1. Product Name: N1-benzyl-N10-(pent-4-ynoyl)tryptamine
    2. Synonyms: N1-benzyl-N10-(pent-4-ynoyl)tryptamine
    3. CAS NO:264619-96-7
    4. Molecular Formula:
    5. Molecular Weight: 330.429
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 264619-96-7.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: N1-benzyl-N10-(pent-4-ynoyl)tryptamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N1-benzyl-N10-(pent-4-ynoyl)tryptamine(264619-96-7)
    11. EPA Substance Registry System: N1-benzyl-N10-(pent-4-ynoyl)tryptamine(264619-96-7)

  • 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: 264619-96-7(Hazardous Substances Data)

264619-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 264619-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,4,6,1 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 264619-96:
(8*2)+(7*6)+(6*4)+(5*6)+(4*1)+(3*9)+(2*9)+(1*6)=167
167 % 10 = 7
So 264619-96-7 is a valid CAS Registry Number.

264619-96-7Relevant articles and documents

Rh-Catalyzed [3 + 2] Cycloaddition of 1-Sulfonyl-1,2,3-triazoles: Access to the Framework of Aspidosperma and Kopsia Indole Alkaloids

Li, Yun,Zhang, Qingyu,Du, Qiucheng,Zhai, Hongbin

, p. 4076 - 4079 (2016)

A Rh(II)-catalyzed dearomative intramolecular [3 + 2] dipolar cycloaddition involving the indolic C2-C3 carbon-carbon double bond has been developed. The reaction was launched from the triazole moiety within the substrate and proceeded efficiently under m

Intramolecular inverse electron demand Diels-Alder reactions of tryptamine with tethered heteroaromatic azadienes

Benson, Scott C.,Lee, Lily,Yang, Lydie,Snyder, John K.

, p. 1165 - 1180 (2007/10/03)

1,2,4,5-Tetrazines and 1,2,4-triazines tethered to tryptamine via the ethylamine side chain undergo intramolecular inverse electron demand cycloadditions to produce adducts with the [ABazaCE]-ring skeleton of the Aspidosperma alkaloids. (C) 2000 Elsevier Science Ltd.

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