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14402-20-1

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14402-20-1 Usage

Chemical Family

Dihydropyridine family

Known as

1-hexadecyl-2-methyl-1,2-dihydropyridine

Biological Activities

Vasodilation and calcium channel blocking

Derivative of

Prototypical dihydropyridine

Potential Applications

Development of novel drug candidates

Target Diseases

Hypertension, heart failure, and neurological disorders

Importance

An important chemical compound with potential therapeutic applications

Check Digit Verification of cas no

The CAS Registry Mumber 14402-20-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,0 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14402-20:
(7*1)+(6*4)+(5*4)+(4*0)+(3*2)+(2*2)+(1*0)=61
61 % 10 = 1
So 14402-20-1 is a valid CAS Registry Number.

14402-20-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hexadecyl-2-methylpyridin-1-ium,iodide

1.2 Other means of identification

Product number -
Other names 1-hexadecyl-2-methyl-pyridinium,iodide

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:14402-20-1 SDS

14402-20-1Relevant articles and documents

Effect of micelle formation of quaternary pyridinium salts on their recyclization to anilines

Stupnikova,Serdyuk,Kalafat,Sagitullin,Marshtupa

, p. 367 - 369 (2007/10/02)

The recyclization of N-alkyl-α-methylpyridinium salts with an N-alkyl chain consisting of 12 and 16 carbon atoms under the influence of aqueous solutions of sulfites of various amines was studied. It was established that the formation of micellar structures in aqueous solutions of these salts affects the direction of the reactions.

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