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17061-62-0

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17061-62-0 Usage

Uses

N,N-Bis(4-methoxybenzyl)amine acts as a reagent for the synthesis and biological evaluation of pentanedioc acid derivatives as farnesyltransferase inhibitors. Also used in the preparation of (heteroarylamino)triazolamines as antiviral agents useful in the treatment of HCV infection.

Check Digit Verification of cas no

The CAS Registry Mumber 17061-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,6 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17061-62:
(7*1)+(6*7)+(5*0)+(4*6)+(3*1)+(2*6)+(1*2)=90
90 % 10 = 0
So 17061-62-0 is a valid CAS Registry Number.
InChI:InChI=1S/C16H19NO2/c1-18-15-7-3-13(4-8-15)11-17-12-14-5-9-16(19-2)10-6-14/h3-10,17H,11-12H2,1-2H3

17061-62-0 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H55180)  Bis(4-methoxybenzyl)amine, 97%   

  • 17061-62-0

  • 250mg

  • 1470.0CNY

  • Detail
  • Alfa Aesar

  • (H55180)  Bis(4-methoxybenzyl)amine, 97%   

  • 17061-62-0

  • 1g

  • 4704.0CNY

  • Detail

17061-62-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Bis(4-methoxybenzyl)amine

1.2 Other means of identification

Product number -
Other names Bis(4-methoxybenzyl)amine

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:17061-62-0 SDS

17061-62-0Relevant articles and documents

Synthesis, spectral, crystal structures, Hirshfeld surface analysis and DFT studies on bis(N,N-di(4-methoxybenzyl)dithiocarbamato-S,S′)zinc(II) and its imine adducts: new precursor for the preparation of hexagonal ZnS

Selvaganapathi, Pandurangan,Thirumaran, Subbiah,Ciattini, Samuele

, p. 655 - 667 (2017)

[Zn(4-mbzdtc)2] (1), [Zn(4-mbzdtc)2(py)] (2), [Zn2(4-mbzdtc)4(4,4′-bipy)] (3), and [Zn(4-mbzdtc)2(2,2′-bipy)] (4), (where, 4-mbzdtc = N,N-di(4-methoxybenzyl)dithiocarbamate) were prepared and characte

Aluminum Metal-Organic Framework-Ligated Single-Site Nickel(II)-Hydride for Heterogeneous Chemoselective Catalysis

Antil, Neha,Kumar, Ajay,Akhtar, Naved,Newar, Rajashree,Begum, Wahida,Dwivedi, Ashutosh,Manna, Kuntal

, p. 3943 - 3957 (2021/04/12)

The development of chemoselective and heterogeneous earth-abundant metal catalysts is essential for environmentally friendly chemical synthesis. We report a highly efficient, chemoselective, and reusable single-site nickel(II) hydride catalyst based on robust and porous aluminum metal-organic frameworks (MOFs) (DUT-5) for hydrogenation of nitro and nitrile compounds to the corresponding amines and hydrogenolysis of aryl ethers under mild conditions. The nickel-hydride catalyst was prepared by the metalation of aluminum hydroxide secondary building units (SBUs) of DUT-5 having the formula of Al(μ2-OH)(bpdc) (bpdc = 4,4′-biphenyldicarboxylate) with NiBr2 followed by a reaction with NaEt3BH. DUT-5-NiH has a broad substrate scope with excellent functional group tolerance in the hydrogenation of aromatic and aliphatic nitro and nitrile compounds under 1 bar H2 and could be recycled and reused at least 10 times. By changing the reaction conditions of the hydrogenation of nitriles, symmetric or unsymmetric secondary amines were also afforded selectively. The experimental and computational studies suggested reversible nitrile coordination to nickel followed by 1,2-insertion of coordinated nitrile into the nickel-hydride bond occurring in the turnover-limiting step. In addition, DUT-5-NiH is also an active catalyst for chemoselective hydrogenolysis of carbon-oxygen bonds in aryl ethers to afford hydrocarbons under atmospheric hydrogen in the absence of any base, which is important for the generation of fuels from biomass. This work highlights the potential of MOF-based single-site earth-abundant metal catalysts for practical and eco-friendly production of chemical feedstocks and biofuels.

Platinum Nanoparticles Uniformly Dispersed on Covalent Organic Framework Supports for Selective Synthesis of Secondary Amines

Li, Xinjun,Liu, Jianguo,Ma, Longlong,Tang, Long,Wang, Chenguang,Wang, Nan

, (2022/01/22)

Covalent organic frameworks (COFs) with pore structures are talented supports for active components. In this report, COF has been rationally fabricated and served as host for growing uniformly dispersed platinum nanoparticles with a narrow size distribution (2 nm). The obtained hybrid Pt/COF exhibits high catalytic activity in the reductive amination of benzaldehyde towards secondary amines with a yield of 96 % and good recyclability. The preferable selectivity towards secondary amines could be attributed to synergistic effects of active platinum nanoparticles and COF, in which metallic Pt nanoparticles were uniformly dispersed with a positively charged surface. This work will open an avenue towards controlling the interaction between active metals and support as well as rational design of catalysts for demanding transformations for fine agrochemicals intermediates.

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