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2H-Pyran-2-amine, tetrahydro-N-(phenylmethyl)-, also known as 2-(benzyl)-tetrahydro-2H-pyran-2-amine, is an organic compound with the molecular formula C12H17NO. It is a derivative of tetrahydro-2H-pyran, a cyclic ether, with a benzyl group attached to the nitrogen atom. 2H-Pyran-2-amine, tetrahydro-N-(phenylmethyl)- is characterized by its amine functional group, which is essential for various chemical reactions and applications. It is used as a building block in the synthesis of more complex organic molecules, particularly in the pharmaceutical and chemical industries. The compound's structure provides a stable platform for further functionalization, making it a valuable intermediate in the creation of drugs, agrochemicals, and other specialty chemicals.

2937-97-5

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2937-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2937-97-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,3 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2937-97:
(6*2)+(5*9)+(4*3)+(3*7)+(2*9)+(1*7)=115
115 % 10 = 5
So 2937-97-5 is a valid CAS Registry Number.

2937-97-5Relevant academic research and scientific papers

Nucleophilic allylation of N,O-acetals with allylic alcohols promoted by Pd/Et3B and Pd/Et2Zn systems

Yamaguchi, Yumi,Hashimoto, Mariko,Tohyama, Katsumi,Kimura, Masanari

supporting information; experimental part, p. 913 - 915 (2011/03/21)

Pd/Et3B and Pd/Et2Zn systems promote the nucleophilic allylations of 2-aminotetrahydrofuran and 2-aminotetrahydropyran with allylic alcohols to provide ω-hydroxyhomoallylamines in high yields. The transformation is applicable to the

Tetrahydropyranylation of alcohols, thiols, phenols and primary amines catalysed by magnesium halide

Goud, P. Mallikarjun,Goud, P. Satish,Reddy, K. Ramasubba,Ashok

, p. 806 - 807 (2007/10/03)

An efficient and mild method for tetrahydropyranylation of thiols, alcohols, phenols and primary amines using a catalytic amount of MgX 2 (X = Br or I) is described; due to the neutral conditions employed, the method is also compatible with com

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