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17165-01-4

1-methyl-2,4-diphenyl-1H-pyrrole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 17165-01-4 Structure

  • Basic information

    1. Product Name: 1-methyl-2,4-diphenyl-1H-pyrrole
    2. Synonyms:
    3. CAS NO:17165-01-4
    4. Molecular Formula: C17H15N
    5. Molecular Weight: 233.3077
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17165-01-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 381.9°C at 760 mmHg
    3. Flash Point: 184.8°C
    4. Appearance: N/A
    5. Density: 1.01g/cm3
    6. Vapor Pressure: 1.08E-05mmHg at 25°C
    7. Refractive Index: 1.582
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-methyl-2,4-diphenyl-1H-pyrrole(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-methyl-2,4-diphenyl-1H-pyrrole(17165-01-4)
    12. EPA Substance Registry System: 1-methyl-2,4-diphenyl-1H-pyrrole(17165-01-4)

  • 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: 17165-01-4(Hazardous Substances Data)

17165-01-4 Usage

Derivative of pyrrole

1-methyl-2,4-diphenyl-1H-pyrrole is derived from pyrrole, which is a heterocyclic aromatic organic compound.

Structure

The compound consists of a pyrrole ring with a methyl group (CH3) and two phenyl groups (C6H5) attached to it.

Potential applications

1-methyl-2,4-diphenyl-1H-pyrrole has potential applications in the fields of organic synthesis and material science.

Versatile intermediate

The compound can be used in the production of pharmaceuticals, agrochemicals, and other fine chemicals.

Unique structure and properties

The compound's structure and properties make it a promising candidate for the development of new materials with specific electronic and optical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 17165-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,6 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17165-01:
(7*1)+(6*7)+(5*1)+(4*6)+(3*5)+(2*0)+(1*1)=94
94 % 10 = 4
So 17165-01-4 is a valid CAS Registry Number.

17165-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-2,4-diphenylpyrrole

1.2 Other means of identification

Product number -
Other names N-methyl-2,4-diphenylpyrrole

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:17165-01-4 SDS

17165-01-4Downstream Products

17165-01-4Relevant articles and documents

Synthesis and Cycloaddition Reactions of Stabilized Münchnones

Kakaawla, Taban K. K.,Hartley, Will C.,Harrity, Joseph P. A.

supporting information, p. 2789 - 2792 (2016/07/07)

A family of stabilized münchnones bearing an acyl group at C4 have been prepared and studied in alkyne cycloaddition reactions. These reactions are highly regioselective, and the method represents a rapid and straightforward route to densely substituted pyrroles. Finally, the C4-stabilizing units can be further manipulated to furnish carboxylic acid and amide groups, or removed altogether to provide unsubstituted pyrroles.

Photochemical reactions of thiobenzamides bearing an allylic substituent on the nitrogen atom: Double-bond migration via tandem 1,4- And 1,6-hydrogen transfer

Aoyama, Hiromu

, p. 1851 - 1854 (2007/10/03)

N-(2-Phenylprop-2-enyl)thiobenzamides 1a-d underwent double-bond migration on irradiation to give N-(2-phenylprop-1-enyl)thiobenzamides 2a-d via consecutive 1,4- and 1,6-hydrogen transfer. Photoreaction of an N-(prop-2-enyl)thiobenzamide 1e and an N-(3-phenylprop-2-enyl)thiobenzamide if did not give migration products, but afforded pyrroles 3e and 3f and dealkylation products 4a in low yields.

1,3-Dipolar Cycloadditions of Nitrones Derived from the Reaction of Acetylenes with Hydroxylamines

Padwa, Albert,Wong, George S. K.

, p. 3125 - 3133 (2007/10/02)

A study of the reaction of hydroxylamines with a variety of acetylenes has been carried out.Methylhydroxylamine readily reacts with methyl propiolate to give methyl 4-carbomethoxy-2-methyl-4-isoxazolidine-3-acetate.Further heating of this material results

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