3-Furancarbinol structure
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Common Name | 3-Furancarbinol | ||
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CAS Number | 4412-91-3 | Molecular Weight | 98.100 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 180.3±0.0 °C at 760 mmHg | |
Molecular Formula | C5H6O2 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 38.3±0.0 °C | |
Symbol |
GHS02, GHS07 |
Signal Word | Warning |
Use of 3-Furancarbinol3-Furanmethanol belongs to the compound class of furan with a wide range of sensory properties. 2-cyanonaphthalenes undergo photocycloaddition reactions with 3-Furanmethanol efficiently and with high degrees of regioselectivity[1][2]. |
Name | 3-Furanmethanol |
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Synonym | More Synonyms |
Description | 3-Furanmethanol belongs to the compound class of furan with a wide range of sensory properties. 2-cyanonaphthalenes undergo photocycloaddition reactions with 3-Furanmethanol efficiently and with high degrees of regioselectivity[1][2]. |
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Related Catalog | |
References |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 180.3±0.0 °C at 760 mmHg |
Molecular Formula | C5H6O2 |
Molecular Weight | 98.100 |
Flash Point | 38.3±0.0 °C |
Exact Mass | 98.036781 |
PSA | 33.37000 |
LogP | 0.20 |
Vapour Pressure | 0.6±0.3 mmHg at 25°C |
Index of Refraction | 1.493 |
Storage condition | Flammables area |
Symbol |
GHS02, GHS07 |
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Signal Word | Warning |
Hazard Statements | H226-H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | Xi |
Risk Phrases | R10;R36/37/38 |
Safety Phrases | S16-S26-S36/37/39-S36/37 |
RIDADR | UN 1987 3/PG 3 |
WGK Germany | 3 |
Packaging Group | III |
Hazard Class | 3.2 |
HS Code | 2932190090 |
HS Code | 2932190090 |
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Summary | 2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0% |
Synthetic Studies Towards the Core Structure of Nakadomarin A by a Thioamide-Based Strategy.
European J. Org. Chem. 2014(1) , 129-39, (2014) The tricyclic BCD substructure of the marine natural product nakadomarin A has been synthesised. The strategy utilised a key carbon-carbon bond-forming reaction between a furan and an N-acyliminium io... |
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Stannylation/destannylation. Preparation of. alpha.-alkoxy organolithium reagents and synthesis of dendrolasin via a carbinyl carbanion equivalent. Still WC.
J. Am. Chem. Soc. 100(5) , 1481-87, (1978)
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3-Alkylfurans as useful synthetic equivalents for substituted δ2-butenolides. Goldsmith D, et al.
Tetrahedron Lett. 24(52) , 5835-38, (1983)
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3-Furylmethanol |
MFCD00005352 |
3-Furanmethanol |
EINECS 224-570-7 |
3-(Hydroxymethyl)furan |
3-Furfuryl alcohol |
furan-3-ylmethanol |
3-Furyl Alcohol |
Furan-3-methanol |
3-Furancarbinol |
3-Furylcarbinol |