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CAS

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140677-17-4

N-(2-(3,4-DIMETHOXYPHENYL)ETHYL)-2-INDOL-3-YL-2-OXOETHANAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 140677-17-4 Structure

  • Basic information

    1. Product Name: N-(2-(3,4-DIMETHOXYPHENYL)ETHYL)-2-INDOL-3-YL-2-OXOETHANAMIDE
    2. Synonyms: N-(2-(3,4-DIMETHOXYPHENYL)ETHYL)-2-INDOL-3-YL-2-OXOETHANAMIDE;N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(1H-indol-3-yl)-2-oxoacetamide
    3. CAS NO:140677-17-4
    4. Molecular Formula: C20H20N2O4
    5. Molecular Weight: 352.38
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 140677-17-4.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-(3,4-DIMETHOXYPHENYL)ETHYL)-2-INDOL-3-YL-2-OXOETHANAMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-(3,4-DIMETHOXYPHENYL)ETHYL)-2-INDOL-3-YL-2-OXOETHANAMIDE(140677-17-4)
    11. EPA Substance Registry System: N-(2-(3,4-DIMETHOXYPHENYL)ETHYL)-2-INDOL-3-YL-2-OXOETHANAMIDE(140677-17-4)

  • 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: 140677-17-4(Hazardous Substances Data)

140677-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140677-17-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,7 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 140677-17:
(8*1)+(7*4)+(6*0)+(5*6)+(4*7)+(3*7)+(2*1)+(1*7)=124
124 % 10 = 4
So 140677-17-4 is a valid CAS Registry Number.

140677-17-4Downstream Products

140677-17-4Relevant articles and documents

Synthesis of marine alkaloid: 8,9-Dihydrocoscinamide B and its analogues as Novel class of antileishmanial agents

Gupta, Leena,Talwar, Archna,Nishi,Palne, Shraddha,Gupta, Suman,Chauhan, Prem M.S.

, p. 4075 - 4079 (2008/02/08)

A series of marine alkaloid 8,9-dihydrocoscinamide B, its analogues and indolylglyoxylamide derivatives have been synthesized and screened for their in vitro antileishmanial activity profile in promastigote and amastigote models. Compounds 7 and 10 have shown 99-100% inhibition against promastigotes and 97-98% inhibition against amastigotes at a concentration of 10 μg/ml.

Benzodiazepine Receptor Affinity and Interaction of Some N-(Indol-3-ylglyoxylyl)amine Derivatives

Bianucci, Anna Maria,Settimo, Antonio Da,Settimo, Federico Da,Primofiore, Giampaolo,Martini, Claudia,et al.

, p. 2214 - 2220 (2007/10/02)

Several derivatives, in which tryptamine, tyramine, and dopamine moieties are linked to the indole nucleus by an oxalyl bridge, were tested for their ability to displace the specific binding of 3H>flunitrazepam from bovine brain membranes.GABA

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