Description

1H,3H-Pyrrolo[1,2-C]Oxazol-1-One,Tetrahydro-3,3-Dimethyl-,(7As)-(9Ci) is a high-purity, specialized heterocyclic building block with significant synthetic utility. This compound is valued for its rigid, fused bicyclic structure, which serves as a key intermediate in the development of complex organic molecules. It is primarily sought after by research and development teams in the pharmaceutical and agrochemical industries for applications in medicinal chemistry and advanced material synthesis.

Application

• Pharmaceutical Intermediate: A crucial chiral synthon for the synthesis of novel active pharmaceutical ingredients (APIs), particularly in neurological and anti-infective drug discovery.
• Agrochemical Research: Used as a building block for developing new generation pesticides and herbicides with enhanced efficacy and selectivity.
• Organic Synthesis Reagent: Employed in academic and industrial R&D for constructing complex heterocyclic frameworks and natural product analogs.
• Material Science Precursor: Potential use in the synthesis of specialized polymers or organic electronic materials due to its unique molecular architecture.
• Chemical Biology Probe Development: Serves as a scaffold for creating molecular probes to study biological pathways and enzyme functions.

Basic Information

Product Name	1H,3H-Pyrrolo[1,2-C]Oxazol-1-One,Tetrahydro-3,3-Dimethyl-,(7As)-(9Ci)
CAS No.	704905-36-2
Molecular Formula	C9H13NO2
Molecular Weight	167.21 g/mol
Synonyms	(7aS)-Tetrahydro-3,3-dimethyl-1H,3H-pyrrolo[1,2-c]oxazol-1-one; (7aS)-3,3-Dimethyltetrahydro-1H,3H-pyrrolo[1,2-c]oxazol-1-one; 1H,3H-Pyrrolo[1,2-c]oxazol-1-one, tetrahydro-3,3-dimethyl-, (7aS)-; 704905-36-2; Pyrrolooxazolone derivative; 3,3-Dimethyltetrahydropyrrolo[1,2-c]oxazol-1(3H)-one
EINECS	Contact for details

Quality Control

Our production of 1H,3H-Pyrrolo[1,2-C]Oxazol-1-One,Tetrahydro-3,3-Dimethyl-,(7As)-(9Ci) adheres to stringent quality management protocols to ensure batch-to-batch consistency and high purity, critical for sensitive R&D and scale-up processes. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We support compliance with cGMP and ISO 9001 standards where required, and specifications can be aligned with client-specific pharmacopeial or internal quality requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to maintain stability and prevent degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Specific Rotation	Contact for details

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