Description

2-Methyl-n-(1R-Naphthalen-1-Yl-Ethyl)-5-Nitrobenzamide is a specialized chiral benzamide derivative, a high-value intermediate in advanced organic synthesis. Its molecular architecture, featuring a naphthyl group and a nitro substituent, makes it a critical building block for constructing complex, biologically active molecules. This compound is essential for research and development chemists in the pharmaceutical and agrochemical industries, particularly for creating novel active ingredients and exploring new chemical entities.

Application

• Pharmaceutical Intermediate: Serves as a key chiral precursor in the synthesis of potential drug candidates, especially for central nervous system (CNS) and anti-inflammatory targets.
• Agrochemical Research: Used in the development of new herbicides, fungicides, and insecticides, leveraging its nitro-aromatic and amide functionalities.
• Ligand Synthesis: Acts as a starting material for creating sophisticated chiral ligands used in asymmetric catalysis.
• Material Science Research: Investigated for the synthesis of organic semiconductors and advanced polymers due to its conjugated naphthalene system.
• Chemical Biology Probes: Utilized in the design of molecular probes for studying enzyme function and biological pathways.

Basic Information

Product Name	2-Methyl-n-(1R-Naphthalen-1-Yl-Ethyl)-5-Nitrobenzamide
CAS No.	1093070-15-5
Molecular Formula	C₂₀H₁₈N₂O₃
Molecular Weight	334.37 g/mol
Synonyms	5-Nitro-2-methyl-N-[(1R)-1-(1-naphthyl)ethyl]benzamide; (R)-N-(1-(Naphthalen-1-yl)ethyl)-2-methyl-5-nitrobenzamide; 2-Methyl-5-nitro-N-[(1R)-1-(1-naphthalenyl)ethyl]benzamide; 2-Methyl-N-[(1R)-1-(1-naphthyl)ethyl]-5-nitrobenzamide; (R)-2-Methyl-N-(1-(naphthalen-1-yl)ethyl)-5-nitrobenzamide; Benzamide, 2-methyl-N-[(1R)-1-(1-naphthalenyl)ethyl]-5-nitro-; CAS 1093070-15-5
EINECS	Contact for details

Quality Control

Our production of 2-Methyl-n-(1R-Naphthalen-1-Yl-Ethyl)-5-Nitrobenzamide adheres to stringent quality management protocols to ensure batch-to-batch consistency and high purity for research and development applications. Each lot is characterized using advanced analytical techniques including HPLC, NMR, and chiral analysis to confirm identity, purity, and enantiomeric excess. Certificates of Analysis (COA) detailing all specifications are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep away from heat, sparks, and open flame. The compound is light-sensitive and should be handled under appropriate conditions to maintain stability.

Specification

Item	Specification
Appearance	Off-white to yellow crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Purity (HPLC)	≥ 97.0%
Enantiomeric Excess (Chiral HPLC)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.