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Glycine, N-[(4-fluoro-3-nitrophenyl)acetyl]is a chemical compound derived from glycine, an essential amino acid crucial for protein synthesis and various biological processes. This derivative features an acetyl group and a 4-fluoro-3-nitrophenyl group attached to the glycine molecule, which may modify its properties and functions. Glycine, N-[(4-fluoro-3-nitrophenyl)acetyl]holds potential for applications in pharmaceuticals, medicinal chemistry, and research focused on amino acid derivatives, although further investigation is required to explore its full capabilities.

192508-38-6

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192508-38-6 Usage

Uses

Used in Pharmaceutical Industry:
Glycine, N-[(4-fluoro-3-nitrophenyl)acetyl]is used as a pharmaceutical intermediate for the development of drugs targeting specific biological processes. The unique structure of Glycine, N-[(4-fluoro-3-nitrophenyl)acetyl]-, with its acetyl and 4-fluoro-3-nitrophenyl groups, may provide novel therapeutic properties and enhance the efficacy of certain medications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, Glycine, N-[(4-fluoro-3-nitrophenyl)acetyl]serves as a valuable research tool for studying the effects of structural modifications on the biological activity of amino acid derivatives. This knowledge can contribute to the design of new drugs with improved pharmacological profiles.
Used in Amino Acid Derivative Research:
Glycine, N-[(4-fluoro-3-nitrophenyl)acetyl]is utilized in research aimed at understanding the role of amino acid derivatives in various biological systems. Glycine, N-[(4-fluoro-3-nitrophenyl)acetyl]-'s distinct chemical structure allows scientists to investigate its interactions with proteins, enzymes, and other biomolecules, potentially uncovering new insights into the mechanisms of action and applications of amino acid-derived compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 192508-38-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,5,0 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 192508-38:
(8*1)+(7*9)+(6*2)+(5*5)+(4*0)+(3*8)+(2*3)+(1*8)=146
146 % 10 = 6
So 192508-38-6 is a valid CAS Registry Number.

192508-38-6SDS

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 2-[[2-(4-fluoro-3-nitrophenyl)acetyl]amino]acetic acid

1.2 Other means of identification

Product number -
Other names <2-(4-fluoro-3-nitrophenyl)-acetylamino>-acetic acid

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:192508-38-6 SDS

192508-38-6Relevant academic research and scientific papers

Synthetic studies towards western and eastern macropolypeptide subunits of Kistamycin

Beugelmans, Rene,Roussi, Georges,Zamora, Eduardo Gonzalez,Carbonnelle, Annie-Claude

, p. 5089 - 5112 (2007/10/03)

The western subunit (fused bicyclic 16+15 membered ring) was synthesized by sequential intramolecular S(N)Ar reaction and the first 17-membered ring compound as model of the eastern subunit was obtained by an intramolecular Ni0 mediated coupling reaction.

The first synthesis of a 15-membered macrocycle. Model of ring I of kistamycin

Roussi, Georges,Zamora, Eduardo Gonzalez,Carbonnelle, Annie-Claude,Beugelmans, Rene

, p. 4405 - 4406 (2007/10/03)

The intramolecular S(N)Ar reaction of a linear peptide precursor, whose termini carry respectively an ortho fluoro-nitro group and a phenol function, gives the 15-membered ring compound in good yield, under mild conditions.

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