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Piperidine, 1-(1,3-diphenyl-2-propynyl)-, also known as 1-(1,3-diphenylprop-2-ynyl)piperidine, is an organic compound with the molecular formula C20H19N. It is a derivative of piperidine, a heterocyclic amine, and features a 1,3-diphenylprop-2-ynyl group attached to the nitrogen atom. Piperidine, 1-(1,3-diphenyl-2-propynyl)- is characterized by its unique structure, which includes a triple bond between the two phenyl rings and the propyne group, making it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its chemical properties and reactivity can be influenced by the presence of the triple bond and the aromatic nature of the phenyl rings, which can participate in various chemical reactions such as addition, substitution, and rearrangement. The compound is typically used in research and development for the creation of new compounds with potential applications in various industries.

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  • 1036-21-1 Structure
  • Basic information

    1. Product Name: Piperidine, 1-(1,3-diphenyl-2-propynyl)-
    2. Synonyms:
    3. CAS NO:1036-21-1
    4. Molecular Formula: C20H21N
    5. Molecular Weight: 275.393
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036-21-1.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: Piperidine, 1-(1,3-diphenyl-2-propynyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Piperidine, 1-(1,3-diphenyl-2-propynyl)-(1036-21-1)
    11. EPA Substance Registry System: Piperidine, 1-(1,3-diphenyl-2-propynyl)-(1036-21-1)
  • 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: 1036-21-1(Hazardous Substances Data)

1036-21-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036-21-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1036-21:
(6*1)+(5*0)+(4*3)+(3*6)+(2*2)+(1*1)=41
41 % 10 = 1
So 1036-21-1 is a valid CAS Registry Number.

1036-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1,3-diphenylprop-2-yn-1-yl)-piperidine

1.2 Other means of identification

Product number -
Other names N-(1,3-diphenyl-2-propyn-1-yl)piperidine

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:1036-21-1 SDS

1036-21-1Relevant articles and documents

Microwave-assisted facile synthesis of propargylamine library by robust nitro functionalized cross-linked polystyrene resin supported Cu NPs

Sharma, Anuj S.,Kaur, Harjinder,Barot, Nirav

, (2018)

In the present investigation, we study catalytic activity of copper nanoparticles stabilized onto a nitro functionalized polystyrene resin (Cu NPs@ Nitro-Resin). The size of stabilized copper nanoparticles was found between 3 and 9?nm. This work reports a

Gold nanoparticles immobilized on lipoic acid functionalized SBA-15: Synthesis, characterization and catalytic applications

Anand, Narani,Ramudu, Pochamoni,Reddy, Kannapu Hari Prasad,Rao, Kamaraju Seetha Rama,Jagadeesh, Bharatam,Babu, Vemulapalli Sahithya Phani,Burri, David Raju

, p. 119 - 126 (2013)

Gold nanoparticles immobilized on lipoic acid functionalized SBA-15 (SBA-LAG) catalyst was synthesized via functionalization of SBA-15 with propylamine followed by tethering of lipoic acid and immobilization of gold nanoparticles. The structural and texct

Heavy metal removing by modified bentonite and study of catalytic activity

Kakaei, Saeed,Khameneh, Elham Sattarzadeh,Rezazadeh, Fardin,Hosseini, Majid Haji

, (2020)

Due to the high hydrophobicity and surface area, clays are efficient adsorbents for the removal of liquid impurities and purification of gases when they are modified. In this work, bentonite was modified with imidazole and imidazolium groups and resulting clays were characterized by different techniques such as 1H NMR, 13C NMR, TEM, SEM, XPS, TG, and FT-IR. Applications of these clays were studied in the removal of Co, Cu, and Pb in the wastewater. Effects of contact time, pH, initial heavy metal ions concentration, and kinetic were investigated. The catalytic activity of the metals adsorbed by imidazole modified bentonite was studied in A3 coupling reactions of various amines, aldehydes, and alkynes.

Magnetically separable ZnFe2O4 nanoparticles: A low cost and sustainable catalyst for propargyl amine and NH-triazole synthesis

Bordoloi, Ankur,Chetia, Swadhin,Garg, Anirban,Guha, Ankur Kanti,Hazarika, Roktopol,Kalita, Amlan Jyoti,Kulshrestha, Akshay,Kumar, Arvind,Phukan, Parmita,Sarma, Diganta

, (2021)

The multicomponent reaction (MCR) strategy for the construction of important molecular scaffolds is in trending nowadays and among them, A3-coupling stands in a significant position. Aldehyde, amine and alkynes are coupled in this particular reaction via C-H activation process. Herein, we have reported zinc ferrite nanoparticles as magnetically separable heterogeneous catalyst for A3-coupling reaction with attractive attributes like excellent productivity, selectivity and better reusability. Moreover, the catalyst can also be effectively applied for the synthesis of various NH-triazoles with quantitative yields of the products. A plausible mechanism has been proposed for the synthesis of NH-triazoles followed by validation with computational study.

Copper modified spherical MCM-41 nano particles: An efficient catalyst for the three-component coupling of aldehydes, amines and alkynes in solvent-free conditions

Abdollahi-Alibeik, Mohammad,Moaddeli, Ali

, p. 39759 - 39766 (2014)

Cu-MCM-41 nano particles have been shown to effectively catalyze the multi-component synthesis of propargylamines by the reaction of aldehydes, amines, and alkynes (A3coupling) effectively at 100 °C under solvent-free conditions. Spherical Cu-M

Fibroin-functionalized magnetic carbon nanotube as a green support for anchoring silver nanoparticles as a biocatalyst for A3 coupling reaction

Akbarzadeh, Parisa,Koukabi, Nadiya

, (2020)

Novel and powerful fibroin-functionalized magnetic carbon nanotube–supported silver nanoparticles (CNT–Fe3O4–fibroin–Ag) were successfully synthesized as a nontoxic and inexpensive biocatalyst. The structure of the organic–inorganic

Solvent-free synthesis of propargylamines via A3 coupling reaction and organic pollutant degradation in aqueous condition using Cu/C catalyst

Rathod, Pramod V.,Puguan, John Marc C.,Kim, Hern

, (2020)

The present report focuses on the efficient and operationally simple synthesis of biomass-derived carbon as support to immobilize copper particles as a catalyst for the one-pot synthesis of propargylamines from furfural via the A3 coupling reaction. This new catalyst showed remarkable catalytic performance leading to a 97% yield within 5 h at 80 °C using 5 mg (0.0022 mmol Cu) of Cu/C catalyst under solvent-free condition. Moreover, nitro-substituted compounds such as 4-nitrophenol (4-NP) are highly toxic and not easily degradable. Hence, a quick and effective method is required to neutralize these toxic compounds. The synthesized active support Cu/C catalyst having various electron-donating groups containing small amounts of Cu plays an essential role in the catalytic reduction of 4-NP (0.1 g). Using only 3 mg (0.0013 mmol Cu) of Cu/C catalyst and NaBH4 (10 mmol), a 99% yield (100% selectivity) in the aqueous condition at 25 °C was achieved. The catalytic reduction follows the pseudo-first-order kinetics with reaction rate constant of 0.028 s?1. Moreover, results demonstrate that the Cu/C catalyst has superior catalytic activity due to the presence of electron-donating molecules such as O, S, and N atoms, which enable synergistic effect in enhancing the overall catalytic performance. Notably, the recoverability and recyclability of the synthesized catalyst were evaluated for up to four cycles, which confirmed its stability in these cycles.

Gold nanoparticle stabilized dithiocarbamate functionalized magnetite carbon as promise clean nanocatalyst for A3-coupling organic transformation

Aghbash, Khadijeh Ojaghi,Alamgholiloo, Hassan,Pesyan, Nader Noroozi,Khaksar, Samad,Rostamnia, Sadegh

, (2021)

A novel, efficient, and core/shell nanosphere catalyst (Fe3O4@C-NHCS-Au0) was successfully synthesized with a movable magnetite core encapsulated in a carbon shell. It was modified using APTES (3-aminopropyltriethoxysilane

Efficient three-component coupling catalysed by mesoporous copper-aluminum based nanocomposites

Dulle, Jana,Thirunavukkarasu,Mittelmeijer-Hazeleger, Marjo C.,Andreeva, Daria V.,Shiju, N. Raveendran,Rothenberg, Gadi

, p. 1238 - 1243 (2013)

Traditional synthesis methods for propargylamines have several drawbacks. A recently developed alternative route is the so-called "A3 coupling" in which an alkyne, an aldehyde, and an amine are coupled together. Typically, these reactions are c

Nafion NR50 catalyzed A3-coupling for the synthesis of propargylamines via C-H activation

Kidwai,Jahan

, p. 462 - 469 (2011)

A one-pot, three-component coupling reaction of aldehydes, amines and alkyne (A3-coupling) via C-H activation using perflorinated resinsulphonic acid (Nafion NR50) as a recyclable and environmentally benign catalyst for the synthesis of proparg

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