Oxetane structure
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Common Name | Oxetane | ||
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CAS Number | 503-30-0 | Molecular Weight | 58.079 | |
Density | 0.9±0.1 g/cm3 | Boiling Point | 49.0±0.0 °C at 760 mmHg | |
Molecular Formula | C3H6O | Melting Point | -97°C | |
MSDS | Chinese USA | Flash Point | -32.0±15.3 °C | |
Symbol |
GHS02, GHS07 |
Signal Word | Danger |
Name | oxetane |
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Synonym | More Synonyms |
Density | 0.9±0.1 g/cm3 |
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Boiling Point | 49.0±0.0 °C at 760 mmHg |
Melting Point | -97°C |
Molecular Formula | C3H6O |
Molecular Weight | 58.079 |
Flash Point | -32.0±15.3 °C |
Exact Mass | 58.041866 |
PSA | 9.23000 |
LogP | -0.24 |
Vapour Pressure | 317.0±0.0 mmHg at 25°C |
Index of Refraction | 1.412 |
Storage condition | 2-8°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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Symbol |
GHS02, GHS07 |
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Signal Word | Danger |
Hazard Statements | H225-H302-H312-H332 |
Precautionary Statements | P210-P280 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US) |
Hazard Codes | F:Highlyflammable;Xn:Harmful; |
Risk Phrases | R11;R20/21/22 |
Safety Phrases | S9-S16-S26-S29 |
RIDADR | UN 1993 3/PG 2 |
WGK Germany | 1 |
RTECS | RQ6825000 |
Packaging Group | II |
Hazard Class | 3 |
HS Code | 2932999099 |
Precursor 9 | |
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DownStream 9 | |
HS Code | 2932999099 |
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Summary | 2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Synthesis of highly substituted oxetanes via [2+2] cycloaddition reactions of allenoates catalyzed by a guanidine Lewis base.
Chem. Commun. (Camb.) 49(28) , 2930-2, (2013) The first synthesis of highly substituted 3-alkyl-oxetan-2-ylidenes from allenoates was developed by using the bicyclic guanidine 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) as an exceptionally active n... |
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A selective intramolecular transacylation of taxoids accompanying with the oxetane ring opening.
Chem. Pharm. Bull. 60(3) , 415-8, (2012) A selective intramolecular transacylation from C-4 to C-5 of taxoids, which occurred simultaneously with the oxetane D-ring opening and was promoted by TiCl4, was presented. The optimal condition was ... |
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Three-component assembly and divergent ring-expansion cascades of functionalized 2-iminooxetanes.
Angew. Chem. Int. Ed. Engl. 49(48) , 9210-4, (2010)
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MFCD00005167 |
Oxacyclobutane |
Trimethylene oxide/Oxetane |
1,3-Epoxypropane |
Trimethylene Oxide |
Oxetane |
Cyclooxabutane |
EINECS 207-964-3 |
Trimethylene oxide (8CI) |