Skip to Content
Merck
All Photos(1)

Key Documents

540366

Sigma-Aldrich

1,1-Diethoxy-3-methyl-2-butene

97%

Sign Into View Organizational & Contract Pricing

Select a Size

5 G
₹10,511.08

₹10,511.08


Available to ship on14 April 2025Details


Request a Bulk Order

Select a Size

Change View
5 G
₹10,511.08

About This Item

Linear Formula:
(C2H5O)2CHCH=C(CH3)2
CAS Number:
Molecular Weight:
158.24
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

₹10,511.08


Available to ship on14 April 2025Details


Request a Bulk Order

Quality Level

Assay

97%

refractive index

n20/D 1.421 (lit.)

bp

53-58 °C/20 mmHg (lit.)

density

0.837 g/mL at 25 °C (lit.)

functional group

ether

SMILES string

CCOC(OCC)\C=C(\C)C

InChI

1S/C9H18O2/c1-5-10-9(11-6-2)7-8(3)4/h7,9H,5-6H2,1-4H3

InChI key

SFUKGEREDDIOED-UHFFFAOYSA-N

General description

1,1-Diethoxy-3-methyl-2-butene is an acyclic alkene.

Application

1,1-Diethoxy-3-methyl-2-butene may be used in the synthesis of:
  • 6,6,10-trimethyl-4-propyl-10,11-dihydro-2H,6H,12H-dipyrano[2,3-f:2′,3′-h]chromene-2,12-dione[1]
  • angular pyranocoumarins[2]
  • 6-cyano-2,2-dimethyl-2-H-1-benzopyran[3]

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

140.0 °F - closed cup

Flash Point(C)

60 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Convenient synthesis of linear pyrano [3, 2-g]-,[2, 3-g]-and angular pyrano [3, 2-f] coumarins from 4 [(1, 1-dimethyl-2-propynyl) oxy] phenol.
Baldoumi, V., et al.
Tetrahedron, 62(34), 8016-8020 (2006)
Tao Ma et al.
Journal of medicinal chemistry, 51(5), 1432-1446 (2008-02-21)
(+)-Calanolide A ( 1) as a natural product was previously found as an inhibitor of HIV-1 reverse transcriptase. In our further investigation of its template, racemic 11-demethyl-12-oxo calanolide A ( 15), which had two fewer chiral carbon centers at the
Green synthesis of 6-cyano-2, 2-dimethyl-2-H-1-benzopyran and its subsequent enantioselective epoxidation.
Romanelli G, et al.
J. Mol. Catal. A: Chem., 398, 11-16 (2015)

Questions

Reviews

No rating value

Active Filters

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