6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene
C11H11FO2
Consulting for 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene
Our experts support you with application, dosage, and compliance.
Identification
- CAS Number
- 99199-90-3
- EC Number
- 419-600-2
- UN Number
- 3082
- Index Number
- 613-227-00-0
- PubChem CID
- 11658439
Physical-chemical properties
- Molecular Formula
- C11H11FO2
- Molar Mass
- 194.20 g/mol
- IUPAC Name
- 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene
Chemical Identifiers
- InChI
- InChI=1S/C11H11FO2/c12-8-2-4-9-7(5-8)1-3-10(14-9)11-6-13-11/h2,4-5,10-11H,1,3,6H2
- InChI Key
- GVZDIJGBXSDSEP-UHFFFAOYSA-N
Overview
6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene (CAS 99199-90-3) is a fluorinated chromene derivative featuring both epoxide and benzopyran structural elements. This specialized organic compound belongs to the chromene family, characterized by its unique combination of a fluorine-substituted benzopyran ring system and a reactive epoxide (oxiran) group. With the molecular formula C11H11FO2 and a molecular weight of 194.2 g/mol, this substance represents an important intermediate in pharmaceutical and fine chemical synthesis. The presence of fluorine at the 6-position of the chromene ring enhances its chemical stability and biological activity profile, while the oxiran-2-yl substituent provides a highly reactive site for further chemical transformations. From a safety perspective, 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene is classified as a skin sensitizer (Skin Sens. 1) and presents chronic aquatic toxicity concerns (Aquatic Chronic 2), requiring appropriate handling precautions. The compound carries a "Warning" signal word and is associated with GHS07 and GHS09 pictograms, indicating both health hazards and environmental concerns. Transportation falls under ADR Class 9 for miscellaneous dangerous goods. Primary industrial applications include its use as a pharmaceutical intermediate in drug development, particularly for compounds requiring fluorinated chromene scaffolds. The compound also serves in specialty polymer synthesis and as a building block for advanced materials research. Unlike simpler structures such as ethyl 6,8-dichlorooctanoate, this chromene derivative offers enhanced reactivity through its epoxide functionality, making it valuable for complex synthetic pathways. OYSI maintains reliable supply chains for this specialized chemical intermediate, supporting pharmaceutical and research applications across European markets.
Safety & Classification
Skin Sens. 1; Aquatic Chronic 2
GHS Pictograms
HHazard Statements (H-Statements)
Describe the nature and severity of the hazard
Classification according to CLP Regulation (EC) No 1272/2008. The complete list of hazard and precautionary statements can be found in the Safety Data Sheet (SDS).
First Aid Measures
Skin Contact
Measures if substance contacts the skin
First Aid Actions
- +P302IF ON SKIN:
- +P352Wash with plenty of water.
- +P361Take off immediately all contaminated clothing.
- +P313Get medical advice/attention.
Related hazard statements:
General Measures
Emergency 112 | Poison Control: +49 30 19240 (DE), +33 1 45 42 59 59 (FR), +31 30 274 88 88 (NL)
First aid measures are based on CLP classification and associated P-statements. They do not replace the Safety Data Sheet (SDS). In case of emergency, always consult the full SDS and a physician.
Transport (ADR)
| UN Number | 3082 |
| ADR Class | 9 |
| Packing Group | III |
| Tunnel Code | - |
| Proper Shipping Name | (+/-)-[(R*,R*) und (R*,S*)]-6-Fluor-3,4-dihydro-2-oxiranyl-2H-1-benzopyran |
| Marine Pollutant | No |
Frequently Asked Questions
What is 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene?
6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene is an organic chemical compound with the molecular formula C11H11FO2 and CAS number 99199-90-3. This fluorinated chromene derivative contains both an epoxide (oxirane) ring and a dihydrochromene structure, giving it unique chemical properties. With a molecular weight of 194.2 g/mol, it is classified as a skin sensitizer and presents chronic aquatic toxicity, requiring careful handling in professional applications.
What are the physicochemical properties of 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene?
6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene is a molecular compound with a molecular weight of 194.2 g/mol and formula C11H11FO2. The presence of fluorine and the epoxide ring significantly influence its reactivity and stability. As a chromene derivative, it likely exists as a liquid or solid at room temperature, though specific physical properties like melting point, boiling point, and solubility data would require detailed technical specifications from suppliers.
What is 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene used for?
6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene serves as an important intermediate in organic synthesis and pharmaceutical research. The compound's epoxide functionality makes it valuable for ring-opening reactions, while the fluorinated chromene structure is useful in medicinal chemistry applications. It may be employed in the development of bioactive compounds, specialty chemicals, or as a building block for more complex molecular structures in research and development laboratories.
How to handle 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene safely?
6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene requires careful handling due to its skin sensitization properties (Skin Sens. 1). Essential personal protective equipment includes chemical-resistant gloves, safety goggles, and protective clothing to prevent skin contact. Work should be conducted in well-ventilated areas or under fume hoods. Avoid direct skin contact and inhalation, and ensure proper training on handling procedures before use. Emergency eyewash and shower facilities should be readily accessible.
How to store 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene correctly?
6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene should be stored in tightly sealed containers in a cool, dry, well-ventilated area away from heat sources and incompatible materials. Due to the reactive epoxide group, avoid exposure to acids, bases, and nucleophiles that could cause ring-opening reactions. Store separately from oxidizing agents and maintain stable temperature conditions. Regular container inspection is recommended, and storage areas should comply with local chemical storage regulations and fire safety requirements.
What to do in case of contact with 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene?
Immediate action is required if contact occurs with 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene due to its skin sensitizing properties. For skin contact, remove contaminated clothing and wash affected area thoroughly with soap and water for at least 15 minutes. If eye contact occurs, rinse immediately with clean water for 15-20 minutes and remove contact lenses if present. Seek medical attention promptly, especially if irritation persists. Keep the safety data sheet available for medical personnel.
How to dispose of 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene appropriately?
6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene must be disposed of through authorized hazardous waste disposal services in accordance with local environmental regulations. Due to its aquatic chronic toxicity (Aquatic Chronic 2), it cannot be discharged into waterways or regular waste streams. Contact licensed chemical waste management companies for proper collection and treatment. Maintain detailed waste disposal records and ensure compliance with national and EU waste management directives including proper waste classification codes.
How to transport 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene?
6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene is classified under ADR Class 9 (Miscellaneous dangerous substances), Packing Group III for transportation purposes. This classification requires appropriate hazardous material packaging, labeling, and documentation during transport. Shipping containers must meet UN specification standards for Packing Group III materials. Transport vehicles require proper placarding, and drivers need hazmat certification. Ensure compliance with international dangerous goods regulations including proper shipping names and emergency response information.
Is 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene subject to special regulations?
6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene is regulated under the European CLP Regulation as indicated by its GHS classification (GHS07, GHS09 pictograms) with 'Warning' signal word. It falls under REACH registration requirements for chemical substances. The compound is not currently listed as a Substance of Very High Concern (SVHC). Users must comply with workplace safety regulations, proper labeling requirements, and maintain safety data sheets. Regular monitoring of regulatory updates is recommended for compliance.
Where to buy 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene in Europe?
6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene is available through OYSI, a specialized European distributor of technical chemicals and pharmaceutical intermediates. OYSI provides professional-grade chemical supplies with proper documentation, safety data sheets, and regulatory compliance support. As experienced chemical distributors, they ensure appropriate packaging, labeling, and transport according to ADR Class 9 requirements. Contact OYSI directly for availability, specifications, and technical support for your specific application requirements.
Services for 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene
Order 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene
Fast delivery across Europe
SDS Service
Request Safety Data Sheet for 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene
Technical Consulting
Application advice for 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene
REACH Safety Data Sheet
REACH Compliance Service
Digital Product Passport
EU-compliant product documentation
ADR Consulting for 6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene
6-fluoro-2-(oxiran-2-yl)-3,4-dihydro-2H-chromene is a dangerous good. We support you with labeling, packaging, and transport documentation.
Data Sources
Classification per CLP Regulation (EC) No 1272/2008. Data from ECHA and PubChem.