3-Furancarbinol

Names

[ Name ]:
3-Furancarbinol

[Synonym ]:
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

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ 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

MSDS

Safety Information

[ Symbol ]:

GHS02, GHS07

[ 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

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2932190090

[ 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%

Articles

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...

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)

3-Alkylfurans as useful synthetic equivalents for substituted δ²-butenolides. Goldsmith D, et al.

Tetrahedron Lett. 24(52) , 5835-38, (1983)

3-benzyl-4-methyl-1,3-thiazol-3-ium,iodide
3-CHLORO-4-(ISOPROPYLSULFONYL)THIOPHENE-2-CARBOXYLIC ACID
3-(1-Benzyl-1H-indol-3-yl)-propionic acid
3,3-diphenyl-4-(2-phenylethenyl)-1-tert-butyl-azetidin-2-one
[3-(4-phenylbenzoyl)phenyl]-(4-phenylphenyl)methanone
3-hydroxy-2,2,4-trimethyl-1-(2-methylphenyl)pentan-1-one
5-Methyl-1-(2-methyl-5-oxocyclohexyl)pyrrolidin-2-one
3-[(2-Tert-butyl-7-chloroquinazolin-4-yl)sulfanyl]propanoic acid
3-{[2-(Ethoxymethyl)-5-fluoroquinazolin-4-yl]sulfanyl}propanoic acid
5-Bromo-6-butyl-2-(propan-2-yl)imidazo[2,1-b][1,3]thiazole
6-Tert-butyl-3-ethylimidazo[2,1-b][1,3]thiazole-5-carboxylic acid
2-[5-ethyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclohexyl]acetic acid
3-Bromo-6-methyl-2-(2-methylpropyl)imidazo[1,2-a]pyridine
3-Bromo-2-tert-butyl-8-ethylimidazo[1,2-a]pyridine
3-Bromo-8-ethyl-2-(1-methylcyclopropyl)imidazo[1,2-a]pyridine
2-Cyclopentyl-7-methylimidazo[1,2-a]pyridine-3-carbaldehyde

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