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N,N-dibenzyl-1-(naphthalen-1-yl)methanamine is a complex organic compound with the molecular formula C26H23N. It is characterized by a naphthalene ring (a fused pair of benzene rings) connected to a methane molecule through an amine group (-NH2). The two benzyl groups (C6H5CH2-) are attached to the nitrogen atom of the amine, which is a common structural feature in many organic compounds. N,N-dibenzyl-1-(naphthalen-1-yl)methanamine is known for its potential applications in the synthesis of pharmaceuticals and other organic materials due to its unique structure and reactivity. It is typically synthesized through various chemical reactions and can be used as a building block for more complex molecules.

5414-88-0

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5414-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5414-88-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5414-88:
(6*5)+(5*4)+(4*1)+(3*4)+(2*8)+(1*8)=90
90 % 10 = 0
So 5414-88-0 is a valid CAS Registry Number.

5414-88-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-N-(naphthalen-1-ylmethyl)-1-phenylmethanamine,hydrochloride

1.2 Other means of identification

Product number -
Other names dibenzyl-[1]naphthylmethyl-amine,hydrochloride

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:5414-88-0 SDS

5414-88-0Upstream product

5414-88-0Downstream Products

5414-88-0Relevant academic research and scientific papers

Amide activation by TMSCl: Reduction of amides to amines by LiAlH 4 under mild conditions

Ravinder,Rajeswar Reddy,Panasa Reddy,Bandichhor, Rakeshwar

supporting information, p. 4908 - 4913 (2013/08/28)

An expeditious and practical method for the reduction of amides to amines is reported. The method consists of activation of amides with TMSCl followed by reduction with LiAlH4. Various amides/lactams including hindered amides and secondary amides gave the corresponding amines in good to excellent yields. This novel protocol has a wide substrate scope and shows good functional group tolerance with high stereoretention.

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