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Acetamide, N-[4-(1-aminoethyl)phenyl]-, (S)is a chemical compound that belongs to the class of organic compounds known as phenylacetamides. These compounds contain a phenylacetamide moiety, which consists of a phenyl group substituted at the nitrogen atom by an acetamide. The "(S)-" in its name signifies the specific spatial arrangement of its atoms, indicating that it is the 'left-handed' version of this molecule. Although not widely studied, the presence of nitrogen, hydrogen, and carbon atoms suggests that Acetamide, N-[4-(1-aminoethyl)phenyl]-, (S)- could participate in various chemical reactions and could potentially be used in a variety of industrial applications.

177947-90-9

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177947-90-9 Usage

Uses

Given the limited information available on Acetamide, N-[4-(1-aminoethyl)phenyl]-, (S)-, it is difficult to definitively list its uses. However, based on its chemical structure and the properties of similar compounds, we can speculate on potential applications:
Used in Chemical Synthesis:
Acetamide, N-[4-(1-aminoethyl)phenyl]-, (S)could be used as a building block or intermediate in the synthesis of more complex organic compounds, particularly those with pharmaceutical or industrial applications.
Used in Pharmaceutical Development:
Due to its unique structure, Acetamide, N-[4-(1-aminoethyl)phenyl]-, (S)may have potential as a starting material for the development of new drugs, especially if it exhibits specific biological activities or interacts with certain biological targets.
Used in Material Science:
Acetamide, N-[4-(1-aminoethyl)phenyl]-, (S)-'s structure may also lend itself to applications in material science, such as the development of new polymers or materials with unique properties.

Check Digit Verification of cas no

The CAS Registry Mumber 177947-90-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,9,4 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 177947-90:
(8*1)+(7*7)+(6*7)+(5*9)+(4*4)+(3*7)+(2*9)+(1*0)=199
199 % 10 = 9
So 177947-90-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2O/c1-7(11)9-3-5-10(6-4-9)12-8(2)13/h3-7H,11H2,1-2H3,(H,12,13)/t7-/m0/s1

177947-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Acetamide, N-[4-(1-aminoethyl)phenyl]-, (S)-

1.2 Other means of identification

Product number -
Other names N-[4-[(1S)-1-aMinoethyl]phenyl]

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:177947-90-9 SDS

177947-90-9Downstream Products

177947-90-9Relevant academic research and scientific papers

3-[3-(piperidin-1-yl)propyl]indoles as highly selective h5-HT(1D) receptor agonists

Russell, Michael G. N.,Matassa, Victor G.,Pengilley, Roy R.,Van Niel, Monique B.,Sohal, Bindi,Watt, Alan P.,Hitzel, Laure,Beer, Margaret S.,Stanton, Josephine A.,Broughton, Howard B.,Castro, José L.

, p. 4981 - 5001 (2007/10/03)

Several 5-HT(ID/1B) receptor agonists are now entering the marketplace as treatments for migraine. This paper describes the development of selective h5-HT(1D)receptor agonists as potential antimigraine agents which may produce fewer side effects. A series of 3-[3-(piperidin-1-yl)propyl]indoles has been synthesized which has led to the identification of 80 (L-772,405), a high- affinity h5-HT(1D) receptor full agonist having 170-fold selectivity for h5- HT(1D) receptors over h5-HT(1B) receptors. L-772,405 also shows very good selectivity over a range of other serotonin and nonserotonin receptors and has excellent bioavailability following subcutaneous administration in rats. It therefore constitutes a valuable tool to delineate the role of h5-HT(1D) receptors in migraine. Molecular modeling and physical properties have been utilized to postulate the binding conformation of these compounds in the receptor cavity.

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