Tetrahydromethyl-1,3-isobenzofurandione
Molecular Structure
Pricing & Availability
Specifications
| Catalog No. | RY207803 |
| CAS No. | 11070-44-3 |
| Molecular Formula | - |
| Molecular Weight | - |
| Purity | 80% mixture of isomers |
| SMILES | NONE |
| MDL Number | MFCD00014585 |
| Category | heterocyclic |
| Storage Condition | Inert atmosphere, room temperature |
| Availability | In Stock |
Synonyms & Alternative Names
Product Description
Tetrahydromethyl-1,3-isobenzofurandione (CAS 11070-44-3) is a high-quality chemical intermediate offered by Raynchem for pharmaceutical, agrochemical, and material science research. The SMILES notation for Tetrahydromethyl-1,3-isobenzofurandione is NONE, representing its complete molecular connectivity for computational chemistry and cheminformatics applications. Our Tetrahydromethyl-1,3-isobenzofurandione is available with a guaranteed purity of 80% mixture of isomers, ensuring consistent and reliable results for your R&D and production needs. Each batch is accompanied by a Certificate of Analysis (COA) verifying identity, purity, and quality. Raynchem provides worldwide fast shipping, competitive pricing, and comprehensive technical support. COA and SDS documents are available upon request. Contact us today for bulk quantities and custom synthesis inquiries.
Applications
- ●Pharmaceutical Intermediate Synthesis: Tetrahydromethyl-1,3-isobenzofurandione (CAS 11070-44-3) serves as a versatile building block in the synthesis of active pharmaceutical ingredients (APIs), enabling the construction of complex molecular architectures through palladium-catalyzed cross-coupling reactions such as Suzuki, Buchwald-Hartwig, and Heck reactions.
- ●Agrochemical Development: This compound is utilized in the preparation of novel agrochemical agents, including herbicides, insecticides, and fungicides, where its halogenated aromatic structure provides key reactivity for further functionalization.
- ●Material Science Research: Tetrahydromethyl-1,3-isobenzofurandione is employed in the development of organic electronic materials, coordination polymers, and functional dyes, where its aromatic amine moiety contributes to optoelectronic properties.
- ●Fine Chemical Manufacturing: Tetrahydromethyl-1,3-isobenzofurandione is suitable for scale-up from milligram to kilogram quantities, supporting both early-stage discovery and late-stage production needs.
Safety & Handling
Hazard Information
- !Tetrahydromethyl-1,3-isobenzofurandione may cause skin irritation (H315) and serious eye irritation (H319).
- !This compound may cause respiratory tract irritation if inhaled.
- !Harmful if swallowed, inhaled, or absorbed through the skin.
- !Contains nitrogen — handle as a potential irritant and avoid formation of nitrogen oxides.
Precautionary Measures
- ✓Wear appropriate personal protective equipment (PPE): chemical-resistant gloves, safety goggles, and laboratory coat.
- ✓Work in a well-ventilated fume hood when handling Tetrahydromethyl-1,3-isobenzofurandione.
- ✓Avoid direct contact with skin, eyes, and clothing. Do not breathe dust, vapors, or aerosols.
- ✓Wash hands thoroughly after handling. Remove contaminated clothing before reuse.
- ✓In case of skin contact: Remove contaminated clothing and wash affected area with plenty of soap and water for at least 15 minutes. Seek medical attention if irritation persists.
- ✓In case of eye contact: Rinse cautiously with water for at least 15 minutes. Remove contact lenses if present. Seek immediate medical attention.
- ✓In case of ingestion: Rinse mouth with water. Do NOT induce vomiting. Seek immediate medical attention.
This information is provided as a general guide. Always consult the Safety Data Sheet (SDS) for complete safety information before handling.
Storage & Stability
- ●Tetrahydromethyl-1,3-isobenzofurandione should be stored inert atmosphere, room temperature.
- ●Keep the container tightly sealed when not in use to prevent degradation and contamination.
- ●Store separately from incompatible materials such as strong oxidizing agents, acids, and bases.
- ●Under proper storage conditions, the shelf life of this product is typically 24 months from the date of manufacture.