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196398

Furan-3-methanol

Name: Furan-3-methanol
Brand: ALDRICH

99%

Synonym(s):

3-(Hydroxymethyl)furan

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About This Item

Empirical Formula (Hill Notation):

C₅H₆O₂

CAS Number:

4412-91-3

Molecular Weight:

98.10

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24851756

EC Number:

224-570-7

Beilstein/REAXYS Number:

106456

MDL number:

MFCD00005352

Assay:

99%

Form:

liquid

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Properties

Quality Level

100

assay

99%

form

liquid

refractive index

n20/D 1.484 (lit.)

bp

79-80 °C/17 mmHg (lit.)

density

1.139 g/mL at 25 °C (lit.)

functional group

hydroxyl

storage temp.

2-8°C

SMILES string

OCc1ccoc1

InChI

1S/C5H6O2/c6-3-5-1-2-7-4-5/h1-2,4,6H,3H2

InChI key

STJIISDMSMJQQK-UHFFFAOYSA-N

Description

General description

Furan-3-methanol on oxidation with pyridinium chlorochromate yields furan-3-carboxaldehyde.

Application

Furan-3-methanol was used in the synthesis of substituted δ²-butenolides and 1-benzyl-3-(furan-3-ylmethyl)-3-methylpyrrolidin-2-one.

pcodes

P210 - P233 - P240 - P280 - P303 + P361 + P353 - P305 + P351 + P338

pictograms

GHS02,GHS07

signalword

Warning

hcodes

H226,H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

flash_point_f

100.4 °F - closed cup

flash_point_c

38 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品

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3-Alkylfurans as useful synthetic equivalents for substituted δ²-butenolides.

Goldsmith D, et al.

Tetrahedron Letters, 24(52), 5835-5838 (1983)

Stannylation/destannylation. Preparation of. alpha.-alkoxy organolithium reagents and synthesis of dendrolasin via a carbinyl carbanion equivalent.

Still WC.

Journal of the American Chemical Society, 100(5), 1481-1487 (1978)

Synthetic Studies Towards the Core Structure of Nakadomarin A by a Thioamide-Based Strategy.

Jai K Chavda et al.

European journal of organic chemistry, 2014(1), 129-139 (2014-05-16)

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

Global Trade Item Number

SKU	GTIN
196398-25G	04061833424223
196398-5G	04061838762047