Skip to Content
MilliporeSigma
All Photos(1)

Documents

217050

Sigma-Aldrich

2-Methoxy-1,3-dioxolane

99%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C4H8O3
CAS Number:
Molecular Weight:
104.10
Beilstein/REAXYS Number:
103177
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

assay

99%

form

liquid

refractive index

n20/D 1.409 (lit.)

bp

129-130 °C (lit.)

density

1.092 g/mL at 25 °C (lit.)

SMILES string

COC1OCCO1

InChI

1S/C4H8O3/c1-5-4-6-2-3-7-4/h4H,2-3H2,1H3

Inchi Key

VRAYTNFBRROPJU-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

application

2-Methoxy-1,3-dioxolane was used in the synthesis of :
  • [4,5-bis(hydroxymethyl)-1,3-dioxolan-2-yl]nucleosides, potential inhibitors of HIV
  • diastereoisomeric cyclic acetals

Pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

93.2 °F - closed cup

flash_point_c

34 °C - closed cup

ppe

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


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Synthesis of highly substituted 2, 6-anti-configured tetrahydropyrans. First steps towards an efficient access to amphidinol 3 ring system.
Dubost C, et al.
Tetrahedron Letters, 46(23), 4005-4009 (2005)
Jonas Brånalt et al.
The Journal of organic chemistry, 61(11), 3599-3603 (1996-05-31)
The synthesis of 1,3-dioxolan-2-ylnucleosides and related chemistry is described. We have shown that 2-methoxy-1,3-dioxolane (6) reacts with silylated thymine and trimethylsilyl triflate to give the acyclic formate ester 1-[2-(formyloxy)ethyl]thymine (8) rather than 1-(1,3-dioxolan-2-yl)thymine (7). A tentative mechanism which could explain

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service