Description

1-Naphthalenecarboxylicacid,1-Amino-1,2,3,4-Tetrahydro-,(1S)-(9Ci) is a chiral, tetrahydro-substituted naphthoic acid derivative that serves as a sophisticated building block in advanced organic synthesis. Its value lies in the precise stereochemistry and functional groups that enable the construction of complex molecular architectures with high enantiomeric purity. This compound is primarily needed by research and development teams in the pharmaceutical and agrochemical industries for creating novel active ingredients, as well as by fine chemical manufacturers specializing in custom synthesis and process development.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the research and development of new active pharmaceutical ingredients (APIs), particularly in therapeutic areas requiring stereospecificity.
• Agrochemical Synthesis: Used in the design and production of advanced, enantiomerically pure herbicides, fungicides, and plant growth regulators.
• Ligand and Catalyst Development: Serves as a precursor for creating novel chiral ligands and organocatalysts used in asymmetric synthesis.
• Material Science Research: Employed in the synthesis of specialty polymers and advanced organic materials with specific optical or electronic properties.
• Academic and Industrial R&D: A valuable tool for chemists in universities and corporate labs exploring new synthetic methodologies and compound libraries.
• Custom Synthesis and Contract Manufacturing: A critical starting material for fine chemical companies offering bespoke synthesis services to the life sciences sector.

Basic Information

Product Name	1-Naphthalenecarboxylicacid,1-Amino-1,2,3,4-Tetrahydro-,(1S)-(9Ci)
CAS No.	197379-82-1
Molecular Formula	C11H13NO2
Molecular Weight	191.23 g/mol
Synonyms	(1S)-1-Amino-1,2,3,4-tetrahydro-1-naphthoic acid; (S)-1-Amino-1,2,3,4-tetrahydro-2-naphthoic acid; 1-Amino-1,2,3,4-tetrahydro-1-naphthoic acid (S-enantiomer); L-1,2,3,4-Tetrahydro-1-amino-1-naphthoic acid; (S)-ATNA; Tetrahydro-1-naphthylglycine derivative; 1,2,3,4-Tetrahydro-1-amino-1-naphthalenecarboxylic acid (S-form)
EINECS	Contact for details

Quality Control

Our production of this advanced chiral intermediate adheres to strict quality management protocols. Each batch is characterized using advanced analytical techniques including HPLC, GC, and NMR to ensure identity, purity, and enantiomeric excess (ee) meet exacting customer requirements. A comprehensive Certificate of Analysis (COA) detailing all specifications is provided with every shipment, ensuring full traceability and compliance with research and cGMP-grade standards where applicable.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after each use to prevent degradation from atmospheric moisture. For long-term storage, consider using desiccants or an inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Enantiomeric Excess (HPLC)	≥ 99.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm

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