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2-(1H-indol-3-ylsulfanyl)-N-[(2E)-1-phenylpyrrolidin-2-ylidene]ethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83747-76-6 Structure
  • Basic information

    1. Product Name: 2-(1H-indol-3-ylsulfanyl)-N-[(2E)-1-phenylpyrrolidin-2-ylidene]ethanamine
    2. Synonyms: ethanamine, 2-(1H-indol-3-ylthio)-N-[(2E)-1-phenyl-2-pyrrolidinylidene]-
    3. CAS NO:83747-76-6
    4. Molecular Formula: C20H21N3S
    5. Molecular Weight: 335.4658
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83747-76-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 538.2°C at 760 mmHg
    3. Flash Point: 279.3°C
    4. Appearance: N/A
    5. Density: 1.21g/cm3
    6. Vapor Pressure: 1.18E-11mmHg at 25°C
    7. Refractive Index: 1.666
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(1H-indol-3-ylsulfanyl)-N-[(2E)-1-phenylpyrrolidin-2-ylidene]ethanamine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(1H-indol-3-ylsulfanyl)-N-[(2E)-1-phenylpyrrolidin-2-ylidene]ethanamine(83747-76-6)
    12. EPA Substance Registry System: 2-(1H-indol-3-ylsulfanyl)-N-[(2E)-1-phenylpyrrolidin-2-ylidene]ethanamine(83747-76-6)
  • 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: 83747-76-6(Hazardous Substances Data)

83747-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83747-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,4 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83747-76:
(7*8)+(6*3)+(5*7)+(4*4)+(3*7)+(2*7)+(1*6)=166
166 % 10 = 6
So 83747-76-6 is a valid CAS Registry Number.

83747-76-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(1H-indol-3-ylsulfanyl)ethyl]-1-phenylpyrrolidin-2-imine

1.2 Other means of identification

Product number -
Other names Mcn 4130

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:83747-76-6 SDS

83747-76-6Downstream Products

83747-76-6Relevant articles and documents

Methods for the treatment of ventricular dysrhythmia and prevention of ventricular fibrillation

-

, (2008/06/13)

Various indole and benzothiophene compounds having a pendant pyrrolidinylidene amino or piperidinylideneamino group are useful in the prevention of ventricular fibrillation, e.g., in humans. The invention comprises methods for the treatment of ventricular

Cardiac-Slowing Amidines Containing the 3-Thioindole Group. Potential Antianginal Agents

Zelesko, Michael J.,McComsey, David F.,Hageman, William E.,Nortey, Samuel O.,Baker, Carol A.,Maryanoff, Bruce E.

, p. 230 - 237 (2007/10/02)

A series of 3-thioindolamidines (and 3-indolamidines) related to mixidine (1) was studied for cardiac-slowing properties, allowing the discovery of activity for prototype thioindole 2.Structure-activity relationships were explored, leading to many potent antitachycardic agents (6-9, 12, 13, 15-17, 20, 23, 24, 30, 34, 35, 45, and 47-49).Relative to 2, cardiac-slowing activity is enhanced by substitution of the indole nitrogen with small (C1-C3) saturated alkyl groups (6-9), unsaturated alkyl groups (12, 13, and 15-17), or a methoxyethyl group (20); replacement of the N-methyl group with alkyl (23) or phenyl groups (24); and extension of the ethylene bridge by two methylene units (34).Dethio (i.e., 3-indole) analogues of 2 with alkyl substitution on the indole nitrogen (47-49) have greater activity as well.Several potent compounds were also found to have minimal myocardial depression (6-9, 13, 45, and 47).Secondary pharmacological testing is reported for thioindoles 2, 6, 7, 9, and 28.

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