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Benzaldehyde, 2-hydroxy-5-methyl-3-[(4-methyl-1-piperazinyl)methyl]-, is a complex organic compound with the chemical formula C16H21N2O2. It is a derivative of benzaldehyde, featuring a hydroxyl group at the 2-position, a methyl group at the 5-position, and a 4-methyl-1-piperazinyl group attached to the 3-position through a methylene bridge. Benzaldehyde, 2-hydroxy-5-methyl-3-[(4-methyl-1-piperazinyl)methyl]- is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs and medicinal compounds. Its structure provides a unique set of functional groups that can be further modified or reacted to create a range of therapeutic agents.

155454-68-5

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155454-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155454-68-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,4,5 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155454-68:
(8*1)+(7*5)+(6*5)+(5*4)+(4*5)+(3*4)+(2*6)+(1*8)=145
145 % 10 = 5
So 155454-68-5 is a valid CAS Registry Number.

155454-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-5-methyl-3-[(4-methylpiperazin-1-yl)methyl]benzaldehyde

1.2 Other means of identification

Product number -
Other names Benzaldehyde,2-hydroxy-5-methyl-3-[(4-methyl-1-piperazinyl)methyl]

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:155454-68-5 SDS

155454-68-5Relevant academic research and scientific papers

A New Method for the Synthesis of Nonsymmetric Dinucleating Ligands by Aminomethylation of Phenols and Salicylaldehydes

Lubben, Marcel,Feringa, Ben L.

, p. 2227 - 2233 (1994)

Monoaminomethylated phenols 5-7 and symmetrically diaminomethylated phenols 8 and 9 were prepared in a one-step procedure from p-cresol, formaldehyde, and a variety of secondary amines by making use of the aromatic Mannich reaction.Nonsymmetric diaminomet

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