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14429-02-8

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14429-02-8 Usage

General Description

Benzyl[(4-methoxyphenyl)methyl]amine is a chemical compound with the molecular formula C15H17NO. It is a derivative of benzylamine, which is a simple aromatic amine. This specific compound features a benzene ring with a benzyl group and a 4-methoxyphenyl group connected to a central amine group. It is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Benzyl[(4-methoxyphenyl)methyl]amine may also have potential applications in medicinal chemistry and drug development due to its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 14429-02-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,2 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14429-02:
(7*1)+(6*4)+(5*4)+(4*2)+(3*9)+(2*0)+(1*2)=88
88 % 10 = 8
So 14429-02-8 is a valid CAS Registry Number.

14429-02-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H55633)  N-Benzyl-4-methoxybenzylamine, 97%   

  • 14429-02-8

  • 250mg

  • 1264.0CNY

  • Detail
  • Alfa Aesar

  • (H55633)  N-Benzyl-4-methoxybenzylamine, 97%   

  • 14429-02-8

  • 1g

  • 4057.0CNY

  • Detail

14429-02-8Relevant articles and documents

Application of odorless thiols for the cleavage of 2- and 4-nitrobenzenesulfonamides

Matoba, Manabu,Kajimoto, Tetsuya,Node, Manabu

, p. 1194 - 1200 (2008)

Several odorless or faint-smelling thiols were tested to cleave 2- and 4-nitrobenzenesulfonyl groups, which are widely utilized for selective protection and activation of amines. p-Mercaptobenzoic acid (7) was found to be the most useful thiol for cleavin

Reductive Alkylation of Azides and Nitroarenes with Alcohols: A Selective Route to Mono- And Dialkylated Amines

Borthakur, Ishani,Maji, Milan,Joshi, Abhisek,Kundu, Sabuj

supporting information, p. 628 - 643 (2021/12/27)

Herein, we demonstrated an efficient protocol for reductive alkylation of azides/nitro compounds via a borrowing hydrogen (BH) method. By following this protocol, selective mono- and dialkylated amines were obtained under mild and solvent-free conditions. A series of control experiments and deuterium-labeling experiments were performed to understand this catalytic process. Mechanistic studies suggested that the Ir(III)-H was the active intermediate in this reaction. KIE study revealed that the breaking of the C-H bond of alcohol might be the rate-limiting step. Notably, this solvent-free strategy disclosed a high TON of around 5600. Based on kinetic studies and control experiments, a metal-ligand cooperative mechanism was proposed.

Polyoxometalate-Driven Ease Conversion of Valuable Furfural to trans- N, N-4,5-Diaminocyclopenten-2-ones

Fountoulaki, Stella,Lykakis, Ioannis N.,Tzani, Marina A.

, (2022/02/10)

We investigated the catalytic efficacy of silicotungstic acid (H4SiW12O40) polyoxometalate (POM) toward the reaction between furfural and amines that selectively yields trans-N,N-4,5-substituted-diaminocyclopenten-2-ones (trans-DACPs). H4SiW12O40 facilita

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