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Benzenemethanol, α-[(propylamino)methyl]-, also known as Propranolol, is a chemical compound with the molecular formula C16H21NO2. It is a non-selective beta-blocker, which means it inhibits the action of certain hormones (such as adrenaline) on the heart, thereby reducing heart rate and blood pressure. Propranolol is primarily used in the treatment of various cardiovascular conditions, including angina, arrhythmias, and hypertension. Additionally, it is prescribed for the management of anxiety, migraines, and certain tremors. The compound is a white crystalline solid and is typically administered orally in tablet form. Propranolol's mechanism of action involves competitive inhibition of beta-adrenergic receptors, which helps to reduce the effects of stress hormones on the heart and blood vessels.

942-94-9

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942-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 942-94-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 942-94:
(5*9)+(4*4)+(3*2)+(2*9)+(1*4)=89
89 % 10 = 9
So 942-94-9 is a valid CAS Registry Number.

942-94-9SDS

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 2-(N-propylamino)-1-phenylethanol

1.2 Other means of identification

Product number -
Other names 1-Phenyl-2-propylamino-aethanol

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:942-94-9 SDS

942-94-9Relevant academic research and scientific papers

Immobilized Pseudomonas sp. lipase: A powerful biocatalyst for asymmetric acylation of (±)-2-amino-1-phenylethanols with vinyl acetate

Yildirim, Deniz,Tükel, S. Seyhan

, p. 819 - 830 (2013/07/27)

Pseudomonas sp. lipase was immobilized onto glutaraldehyde-activated Florisil support via Schiff base formation and stabilized by reducing Schiff base with sodium cyanoborohydride. The immobilization performance was evaluated in terms of bound

Design and synthesis of a functionally selective D3 agonist and its in vivo delivery via the intranasal route

Blagg, Julian,Allerton, Charlotte M.N.,Batchelor, David V.J.,Baxter, Andrew D.,Burring, Denise J.,Carr, Christopher L.,Cook, Andrew S.,Nichols, Carly L.,Phipps, Joanne,Sanderson, Vivienne G.,Verrier, Hugh,Wong, Stephen

, p. 6691 - 6696 (2008/03/14)

This paper reports the synthesis and biological activity of a novel series of aryl-morpholine dopamine receptor agonists. Several compounds show high levels of functional selectivity for the D3 over the D2 dopamine receptor. Compound 26 has >1000-fold functional selectivity and has been successfully progressed in vivo using an intranasal delivery route.

BiCl3-mediated opening of epoxides, a facile route to chlorohydrins or amino alcohols: One reagent, two paths

McCluskey, Adam,Leitch, Sarah K.,Garner, James,Caden, Christine E.,Hill, Timothy A.,Odell, Luke R.,Stewart, Scott G.

, p. 8229 - 8232 (2007/10/03)

Opening of epoxides can be an effective means by which a variety of functional groups can be incorporated. In this letter, we outline how variation of conditions, in particular, that of solvent and concentration, give rise to different products using the Lewis acid catalyst BiCl3.

The selective preparation of n-propylamines by the rhodium catalysed reaction of ethylene and syngas with alkylamines

Jones, M. D.

, p. 403 - 408 (2007/10/02)

The aminoethylation of ethylene with a primary amine has been shown to provide a highly selective route to n-propylamines; the rhodium catalysed reaction of n-propylamine with ethylene and syngas (2/1, H2/CO) affords di-n-propylamine with 98percent selectivity (with respect to ethylene).The reaction of amines of the type RR1NH with the ethylene/syngas mixture and a rhodium catalyst provides a highly selective and general route to the n-propylamines RR1NPr (R=Pr, R1=H; R=t-Bu, R1=H; R=n-Bu, R1=H; R=C8H17, R1=H, R=R1=Pr; R=HOCH2Ch2, R1=H, and R=PhCH(OH)CH2, R1=H).

The Reaction of Phenylglyoxal with Primary Aliphatic and Aromatic Amines. Synthesis of Phenylglyoxal Monoimines and some Derivatives.

Alcaide, Benito,Escobar, Gerardo,Perez-Ossorio, Rafael,Plumet, Joaquin,Sanz, Dionisia

, p. 1466 - 1488 (2007/10/02)

Condensation of phenylglyoxal with primary aliphatic amines yields the related keto-aldimines.When primary aromatic amines are used, aldimines, amino-hydroxy-ketones, diamino-ketones, and alkoxy-amino-ketones are obtained depending upon the nature of the amine and the experimental conditions.Alternatively the monoimines can be obtained by dehydration of C-hydroxyphenacylarylamines and by demethanolation of C-methoxyphenacylarylamines both on treatment with Pd/C catalyst.Reduction of phenylglyoxal monoimines with sodium borohydride yielded H-substituted 1-phenyl-2-aminoethanols and 1,3-dipolar cycloaddition of the imines with p-chlorobenzonitrile oxide afforded 4-substituted 5-benzoyl-3-(p-chlorophenyl)-4,5-dihydro-1,2,4-oxadiazoles.

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