Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C3H6O2
CAS Number:
Molecular Weight:
74.08
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
102453
MDL number:
Assay:
≥99.5%
Bp:
75-76 °C/1.013 hPa
Vapor pressure:
70 mmHg ( 20 °C)
vapor density
2.6 (vs air)
vapor pressure
70 mmHg ( 20 °C)
assay
≥99.5%
autoignition temp.
525 °F
contains
75 ppm BHT as inhibitor
refractive index
n20/D 1.401 (lit.)
bp
75-76 °C/1.013 hPa
mp
−95 °C (lit.)
density
1.06 g/mL at 25 °C (lit.)
SMILES string
C1COCO1
InChI
1S/C3H6O2/c1-2-5-3-4-1/h1-3H2
InChI key
WNXJIVFYUVYPPR-UHFFFAOYSA-N
Still not finding the right product?
Explore all of our products under 1,3-Dioxolane
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Benito Alcaide et al.
The Journal of organic chemistry, 78(18), 8956-8965 (2013-09-07)
The gold-catalyzed preparation of 2-azetidinone-fused oxacycles was accomplished from β-lactam-linked enynes through heterocyclization reaction taking advantage of the acetonide pendant group. While the synthesis of fused tetrahydrofuran-β-lactams from 1,3-enynes could be considered as an unusual metal-catalyzed cyclization of enynols, α-alkoxy
Matthias Schmidt et al.
Bioorganic & medicinal chemistry, 15(6), 2283-2297 (2007-02-06)
Multidrug resistance (MDR) to antitumor agents represents a major obstacle to a successful chemotherapy of cancer. Overexpression of P-glycoprotein (p-gp) seems to be the major factor responsible for MDR. A large number of chemically unrelated compounds are known to interact
Benjamin L Wegenhart et al.
Inorganic chemistry, 49(11), 4741-4743 (2010-05-06)
Low catalyst loading of a cationic oxorhenium(V) oxazoline complex, [2-(2'-hydroxyphenyl)-2-oxazolinato(-2)]oxorhenium(v), condenses diols and aldehydes to give 1,3-dioxolanes in excellent yields under neat conditions and reasonably mild temperatures. The reaction is applicable to biomass-derived furfural and glycerol. The resulting cyclic acetals