Skip to Content
Merck
CN

245100

2,2,6-Trimethyl-4H-1,3-dioxin-4-one

95%

Synonym(s):

Diketene acetone adduct

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C7H10O3
CAS Number:
Molecular Weight:
142.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2408
Assay:
95%
Form:
liquid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


Quality Segment

assay

95%

form

liquid

refractive index

n20/D 1.460 (lit.)

bp

~275 °C (lit.), 65-67 °C/2 mmHg (lit.)

mp

12-13 °C (lit.)

solubility

water: insoluble

density

1.07 g/mL at 25 °C (lit.)

functional group

ester, ether, ketal

SMILES string

CC1=CC(=O)OC(C)(C)O1

InChI

1S/C7H10O3/c1-5-4-6(8)10-7(2,3)9-5/h4H,1-3H3

InChI key

XFRBXZCBOYNMJP-UHFFFAOYSA-N

General description

2,2,6-Trimethyl-4H-1,3-dioxin-4-one is used as a building block in organic synthesis and serves as a direct precursor to β-dicarbonyl compounds

Application

2,2,6-Trimethyl-4H-1,3-dioxin-4-one was used in the synthesis of acetylketene by flash pyrolysis.

Other Notes

remainder acetone


Still not finding the right product?


pictograms

FlameExclamation mark

Storage Class

3 - Flammable liquids

wgk

WGK 1

ppe

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

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3

flash_point_f

75.2 °F - closed cup

flash_point_c

24 °C - closed cup

signalword

Warning

hcodes

Regulatory Information

新产品

This item has



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



2, 2, 6-Trimethyl-4H-1, 3-dioxin-4-one
M Seyyedhamzeh, et al.
Synlett, 23, 1556-1557 (2012)
David M. Birney et al.
The Journal of organic chemistry, 62(21), 7114-7120 (2001-10-24)
Acetylketene (1) was generated by flash pyrolysis of 2,2,6-trimethyl-4H-1,3-dioxin-4-one (6). The selectivities of 1 toward a number of representative functional groups were measured for the first time in a series of competitive trapping reactions. The trend in reactivities toward 1



Global Trade Item Number

SKUGTIN
245100-100G04061825772455