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2-[[2-(Carbamoylmethylamino)ethoxy]methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methylpyridine-3,5-dicarboxylic acid 3-ethyl 5-methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88150-59-8

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88150-59-8 Usage

Molecular structure

The compound contains a pyridine ring, which is a six-membered heterocyclic aromatic ring with one nitrogen atom.

Carbamoylmethylamino group

The compound has a carbamoylmethylamino group (-NHCOCH3), which is derived from the reaction of an amine with carbon dioxide. This group can participate in hydrogen bonding and may be involved in biological activity.

Ethyl 5-methyl ester group

The compound features an ethyl 5-methyl ester group (-COOCH2CH3), which is an ester formed from the reaction of a carboxylic acid with an alcohol. This group can influence the compound's solubility and may be involved in metabolic processes.

2-chlorophenyl group

A 2-chlorophenyl group (-C6H4Cl) is attached to the pyridine ring, which introduces a chlorine atom to the compound and may affect its lipophilicity, electronic properties, and biological activity.

Potential medical applications

Due to its complex structure and various functional groups, the compound may have potential medical or pharmaceutical applications, such as serving as a building block for the development of new drugs or as a research tool in pharmacology and medicinal chemistry.

Biological activity

The presence of multiple functional groups in the compound suggests that it may have biological activity, potentially interacting with proteins, enzymes, or other biomolecules in living organisms.

Solubility

The compound's solubility may be influenced by its functional groups, such as the ethyl 5-methyl ester group, which can affect its absorption, distribution, and elimination in biological systems.

Stability

The compound's stability may be affected by its functional groups and the presence of the pyridine ring, which can contribute to its resistance to chemical reactions and degradation.

Synthesis

The compound's complex structure suggests that its synthesis may involve multiple steps and reactions, potentially requiring the use of various reagents and catalysts.

Check Digit Verification of cas no

The CAS Registry Mumber 88150-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,5 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88150-59:
(7*8)+(6*8)+(5*1)+(4*5)+(3*0)+(2*5)+(1*9)=148
148 % 10 = 8
So 88150-59-8 is a valid CAS Registry Number.

88150-59-8SDS

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 UK-51656

1.2 Other means of identification

Product number -
Other names 2-(2-{[4-(2-Chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyrid-2-yl]methoxy}ethylamino)acetamide

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:88150-59-8 SDS

88150-59-8Downstream Products

88150-59-8Relevant academic research and scientific papers

Long-Acting Dihydropyridine Calcium Antagonists. 4. Synthesis and Structure-Activity Relationships for a Series of Basic and Nonbasic Derivatives of 2--1,4-dihydropyridine Calcium Antagonists

Alker, David,Campbell, Simon F.,Cross, Peter E.,Burges, Roger A.,Carter, Anthony J.,Gardiner, Donald G.

, p. 585 - 591 (2007/10/02)

The preparation of a series of 1,4-dihydropyridines (DHPs) which have polar, acyclic, nonbasic substituents on an ethoxymethyl chain at the 2-position is described.In addition, in order to assess the effects of incorporating a basic center into DHPs of th

2-(SECONDARY AMINOALKOXYMETHYL) DIHYDROPYRIDINE DERIVATIVES AS ANTI-ISCHAEMIC AND ANTIHYPERTENSIVE AGENTS

-

, (2008/06/13)

A dihydropyridine compound of the formula or a pharmaceutically acceptable acid addition salt thereof, wherein Y is -(CH2)2-, -(CH2)3-, -CH2CH(CH3)-or -CH2C(CH3)2-; R is aryl or heteroaryl; R1 and R2 are each independently C1-C4 alkyl or 2-methoxyethyl; and R3 is hydrogen, C1-C4 alkyl, 2-(Ci-C4 alkoxy)ethyl, cyclopropylmethyl, benzyl, or -(CH2)mCOR4 where m is 1, 2 or 3 and R4 is hydroxy, C1-C4 alkoxy or -NR5R6 where R5 and R6 are each independently hydrogen or C1-C4 alkyl can be employed for treating or preventing a heart condition or hypertension.

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