3129-54-2

Basic information

• Product Name: N-2,4-DNP-SARCOSINE
• Synonyms: SPECS AR-299/42656434;N-2,4-DNP-SARCOSINE;dnp-sarcosine;n-(2,4-dinitrophenyl)-sarcosine;2-(N-methyl-2,4-dinitroanilino)acetic acid;2-(N-methyl-2,4-dinitro-anilino)acetic acid;2-[(2,4-dinitrophenyl)-methyl-amino]ethanoic acid
• CAS NO: 3129-54-2
• Molecular Formula: C₉H₉N₃O₆
• Molecular Weight: 255.18
• Mol File: 3129-54-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 482 °C at 760 mmHg
• Flash Point: 245.3 °C
• Appearance: /
• Density: 1.572 g/cm³
• Vapor Pressure: 4.2E-10mmHg at 25°C
• Refractive Index: 1.659
• Storage Temp.: −20°C
• CAS DataBase Reference: N-2,4-DNP-SARCOSINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-2,4-DNP-SARCOSINE(3129-54-2)
• EPA Substance Registry System: N-2,4-DNP-SARCOSINE(3129-54-2)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 3129-54-2(Hazardous Substances Data)

Usage

Description

N-2,4-DNP-SARCOSINE is a chemical compound that consists of a sarcosine molecule linked to a dinitrophenyl (DNP) group. Sarcosine is a naturally occurring amino acid that is found in certain foods and is also synthesized in the human body. It is believed to play a role in the metabolism of fatty acids and the production of energy. The addition of the DNP group to sarcosine creates a derivative that can be used in chemical analysis and research, particularly in the study of amino acids and related compounds. The DNP group also imparts certain properties to the compound that may make it useful in other applications, such as in the development of pharmaceuticals or other molecular tools.

Uses

Used in Chemical Analysis and Research:
N-2,4-DNP-SARCOSINE is used as a chemical probe for the study of amino acids and related compounds. Its unique structure allows researchers to investigate the interactions and properties of sarcosine and other amino acids in various chemical and biological systems.
Used in Pharmaceutical Development:
N-2,4-DNP-SARCOSINE is used as a potential lead compound in the development of pharmaceuticals. The DNP group imparts certain properties to the compound that may enhance its therapeutic potential, making it a valuable tool in the discovery and optimization of new drugs.
Used in Molecular Tools Development:
N-2,4-DNP-SARCOSINE is used as a component in the development of molecular tools for various applications. Its unique structure and properties make it a promising candidate for the creation of new reagents, probes, and other tools that can be used in research and industry.

InChI:InChI=1/C9H9N3O6/c1-10(5-9(13)14)7-3-2-6(11(15)16)4-8(7)12(17)18/h2-4H,5H2,1H3,(H,13,14)

Upstream product

• 107-97-1 sarcosine 
• 70-34-8 2,4-Dinitrofluorobenzene 
• 97-00-7 1-chloro-2,4-dinitro-benzene 

Downstream Products

• 116059-06-4 N-methyl-N-(2,4-dinitrophenyl)glycine ethyl ester 
• 124552-68-7 2-acetamido-2'-(N-methylacetamido)-5,5'-dinitro-ONN-azoxybenzene 
• 119548-63-9 2,2'-bis(methylamino)-5,5'-dinitroazoxybenzene 
• 116059-13-3 2-amino-2'-methylamino-5,5'-dinitro-ONN-azoxybenzene 

Relevant articles and documents

Synthesis of tri- and tetracyclic condensed quinoxalin-2-ones fused across the C-3 - N-4 bond

We have studied the preparation of some fused quinoxalinones by Stevens rearrangement of a spiro-quinoxaline-derived ammonium ylide or by treatment of N-(2,4-dinitrophenyl)-and N-(2-nitrophenyl)imino acids with different reducing agents. We have reinvestigated and clarified some related processes found in the literature starting from imino acids derivatives. Additional reactions of the fused quinoxalinones, as well as the useful dehydrogenation/decarboxylation of some easily available 1-arylindoline-2-carboxylic acids to the corresponding 1-arylindoles, are also reported. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.