Description

1H-Indene-1-Carboxaldehyde, 2,3-Dihydro-, (1R)- (9Ci) is a chiral, high-purity organic building block of significant interest in advanced synthetic chemistry. Its defined stereochemistry and reactive aldehyde functional group make it a critical intermediate for constructing complex molecular architectures. This compound is primarily sought after by research institutions and pharmaceutical developers for applications in asymmetric synthesis, medicinal chemistry, and the development of novel active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical Intermediate: A key chiral synthon in the research and development of new therapeutic agents and active pharmaceutical ingredients (APIs).
• Asymmetric Synthesis: Used as a building block for constructing complex, enantiomerically pure molecules in academic and industrial research.
• Medicinal Chemistry & Drug Discovery: Employed in lead optimization and structure-activity relationship (SAR) studies to develop novel drug candidates.
• Ligand and Catalyst Development: Serves as a precursor for synthesizing chiral ligands and organocatalysts used in stereoselective transformations.
• Fine Chemical Synthesis: Utilized in the multi-step synthesis of specialty chemicals, flavors, and fragrances requiring high stereochemical purity.
• Academic Research: A valuable reagent for methodological studies in organic synthesis and stereochemistry.

Basic Information

Item	Detail
Product Name	1H-Indene-1-Carboxaldehyde, 2,3-Dihydro-, (1R)- (9Ci)
CAS No.	500723-14-8
Molecular Formula	C10H10O
Molecular Weight	146.19 g/mol
Synonyms	(1R)-2,3-Dihydro-1H-indene-1-carboxaldehyde; (R)-2,3-Dihydro-1H-indene-1-carbaldehyde; (R)-Indane-1-carbaldehyde; (1R)-Indan-1-carboxaldehyde; (R)-1-Formylindane; (R)-1-Indanecarboxaldehyde; (R)-1-Indanecarbaldehyde; (R)-α-Formylindane
EINECS	Contact for details

Quality Control

Our production of 1H-Indene-1-Carboxaldehyde, 2,3-Dihydro-, (1R)- (9Ci) adheres to stringent quality protocols to ensure batch-to-batch consistency and high enantiomeric purity. Each lot is characterized by advanced analytical techniques including chiral HPLC, NMR, and GC-MS. A comprehensive Certificate of Analysis (COA) detailing identity, purity, chiral excess, and impurity profile is provided with every shipment, supporting your regulatory and research documentation needs.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) at controlled room temperature (15-25°C) in a cool, dry, and well-ventilated area. This material is easily oxidized and light-sensitive; prolonged exposure to air or light should be avoided to maintain stability and purity.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid or low-melting solid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Chiral Purity (Chiral HPLC)	≥ 98.0% e.e.
Water Content (KF)	≤ 0.5%

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