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836-41-9

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836-41-9 Usage

General Description

N-(4-Methoxybenzylidene)aniline is a chemical compound with the molecular formula C14H13NO. It is a yellowish crystalline solid that is commonly used in the synthesis of organic compounds. This chemical is also utilized in the production of dyes and pigments due to its ability to impart color to materials. N-(4-Methoxybenzylidene)aniline is known for its aromatic properties and is often used as a building block in the pharmaceutical and chemical industries. Additionally, it has been researched for its potential biological activities and medicinal properties. However, it is important to handle N-(4-Methoxybenzylidene)aniline with caution, as it can be harmful if ingested or inhaled, and may cause irritation to the skin and eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 836-41-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 836-41:
(5*8)+(4*3)+(3*6)+(2*4)+(1*1)=79
79 % 10 = 9
So 836-41-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO/c1-16-14-9-7-12(8-10-14)11-15-13-5-3-2-4-6-13/h2-11H,1H3

836-41-9 Well-known Company Product Price

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  • Alfa Aesar

  • (L01951)  N-(4-Methoxybenzylidene)aniline, 98%   

  • 836-41-9

  • 5g

  • 382.0CNY

  • Detail
  • Alfa Aesar

  • (L01951)  N-(4-Methoxybenzylidene)aniline, 98%   

  • 836-41-9

  • 25g

  • 1326.0CNY

  • Detail
  • Aldrich

  • (680362)  N-(4-Methoxybenzylidene)aniline  97%

  • 836-41-9

  • 680362-5G

  • 332.28CNY

  • Detail
  • Aldrich

  • (680362)  N-(4-Methoxybenzylidene)aniline  97%

  • 836-41-9

  • 680362-25G

  • 1,016.73CNY

  • Detail

836-41-9SDS

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-(4-Methoxybenzylidene)aniline

1.2 Other means of identification

Product number -
Other names N-(4-METHOXYBENZYLIDENE)ANILINE

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:836-41-9 SDS

836-41-9Relevant articles and documents

β-Lactams (including polycyclic) derived from chromium carbenes

Woodgate, Paul D.,Sutherland, Hamish S.,Rickard, Clifton E.F.

, p. 114 - 130 (2001)

The photolytic reaction of N-methylbenzylideneimine with 12-methoxypodocarpane chromium carbenes gave products derived either from carbon monoxide dissociation followed by 12-methoxy ligation or from oxidation of the carbene metal moiety, while the reacti

Half-sandwich Ru(ii) arene complexes bearing benzimidazole ligands for theN-alkylation reaction of aniline with alcohols in a solvent-free medium

?i?ek, Metin,Gürbüz, Nevin,?zdemir, Nam?k,?zdemir, ?smail,?spir, Esin

, p. 11075 - 11085 (2021/07/02)

In this article, the directN-alkylation reactions of amines with alcohol derivatives using the borrowing hydrogen methodology have been investigated. For this purpose, a new series of half-sandwich ruthenium(ii) complexes bearing N-coordinated benzimidazole complexes have been synthesized and fully characterized by FT-IR,1H NMR and13C NMR spectroscopies. Additionally, the structures of the complexes2a-2ehave been characterized by X-ray crystallography. All new complexes were investigated for their catalytic activities in the alkylation reaction of amines with alcohol derivatives. It was found that alkylation reactions in a solvent-free medium are efficient and selective.

Efficient Imine Formation by Oxidative Coupling at Low Temperature Catalyzed by High-Surface-Area Mesoporous CeO2 with Exceptional Redox Property

Wu, Shipeng,Wang, Yinghao,Cao, Qiue,Zhao, Qihua,Fang, Wenhao

supporting information, p. 3019 - 3028 (2020/12/11)

High-surface-area mesoporous CeO2 (hsmCeO2) was prepared by a facile organic-template-induced homogeneous precipitation process and showed excellent catalytic activity in imine synthesis in the absence of base from primary alcohols and amines in air atmosphere at low temperature. For comparison, ordinary CeO2 and hsmCeO2 after different thermal treatments were also investigated. XRD, N2 physisorption, UV-Raman, H2 temperature-programmed reduction, O2 temperature-programmed desorption, EPR spectroscopy, and X-ray photoelectron spectroscopy were used to unravel the structural and redox properties. The hsmCeO2 calcined at 400 °C shows the highest specific surface area (158 m2 g?1), the highest fraction of surface coordinatively unsaturated Ce3+ ions (18.2 %), and the highest concentration of reactive oxygen vacancies (2.4×1015 spins g?1). In the model reaction of oxidative coupling of benzyl alcohol and aniline, such an exceptional redox property of the hsmCeO2 catalyst can boost benzylideneaniline formation (2.75 and 5.55 mmol (Formula presented.) h?1 based on >99 % yield at 60 and 80 °C, respectively) in air with no base additives. It can also work effectively at a temperature of 30 °C and in gram-scale synthesis. These are among the best results for all benchmark ceria catalysts in the literature. Moreover, the hsmCeO2 catalyst shows a wide scope towards primary alcohols and amines with good to excellent yield of imines. The influence of reaction parameters, the reusability of the catalyst, and the reaction mechanism were investigated.

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