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3-(4-allyl-2-methoxyphenoxy)-1,2-propanediol, also known as propranolol, is a chemical compound with the molecular formula C10H15NO3. It is a white crystalline powder that is soluble in water and has a molecular weight of 193.23 g/mol. 3-(4-allyl-2-methoxyphenoxy)-1,2-propanediol is primarily used as a non-selective beta-blocker, which is a type of medication that helps to treat various cardiovascular conditions, such as hypertension, angina, and arrhythmias. Propranolol works by blocking the action of certain hormones and neurotransmitters on the heart, thereby reducing heart rate and blood pressure. It is also used to treat anxiety disorders and prevent migraines. The chemical structure of propranolol consists of a propanediol backbone with a 4-allyl-2-methoxyphenoxy group attached to the third carbon, which contributes to its pharmacological properties.

398-58-3

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398-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 398-58-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 398-58:
(5*3)+(4*9)+(3*8)+(2*5)+(1*8)=93
93 % 10 = 3
So 398-58-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O4/c1-3-4-10-5-6-12(13(7-10)16-2)17-9-11(15)8-14/h3-7,11,14-15H,8-9H2,1-2H3/b4-3+

398-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-allyl-2-methoxyphenoxy)-1,2-propanediol

1.2 Other means of identification

Product number -
Other names 3-Methoxy-1-allyl-4-phenoxypropandiol

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:398-58-3 SDS

398-58-3Relevant academic research and scientific papers

Crown ether compositions with sidearms affording enhanced cation binding

-

, (2008/06/13)

This invention relates to novel crown ether compositions which have been given the cognomen "lariat ethers". They have been designed with one or more arms bearing neutral donor groups capable of interacting with a complexed metal ion and thereby affording enhanced cation binding compared to simple crown ethers. Evidence of enhanced cation binding has been obtained and the compounds have also shown utility as phase transfer catalysts.

Crown Cation Complex Effects. 20. Syntheses and Cation Binding Properties of Carbon-Pivot Lariat Ethers

Dishong, Dennis M.,Diamond, Craig J.,Cinoman, Michael I.,Gokel, Geoge W.

, p. 586 - 593 (2007/10/02)

In an effort devise synthetic cation binders that will mimic the behavior of naturally occuring ionophores such as valinomycin, we have prepared approximately 30 macrocyclic (crown) polyethers bearing flexible side chains attached to the macro ring at carbon.In many of these "carbon-pivot" compounds, the side chain contains one or more neutral donor groups that, if in a suitable geometrical arrangement, may provide additional solvation to the macro-ring-bound cation.Although such donors often enhanced the cation binding ability, overall, the increases in stability constants were modest.The physical resemblance and concept of "roping and tying" the cation suggest the name "lariat ethers".Syntheses of these molecules and binding by them of Na+ and K+ cations are reported and conclusions drawn about the structural requirements and cation binding efficacy of these materials.

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