Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

119865

Sigma-Aldrich

4′-Morpholinoacetophenone

99%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C12H15NO2
CAS Number:
39910-98-0
Molecular Weight:
205.25
EC Number:
254-698-9
MDL number:
MFCD00006168
UNSPSC Code:
12352100
PubChem Substance ID:
24847301
NACRES:
NA.22

Assay

99%

mp

96-98 °C (lit.)

functional group

ether
ketone

SMILES string

CC(=O)c1ccc(cc1)N2CCOCC2

InChI

1S/C12H15NO2/c1-10(14)11-2-4-12(5-3-11)13-6-8-15-9-7-13/h2-5H,6-9H2,1H3

InChI key

AKQWEDMTPCAESO-UHFFFAOYSA-N

General description

4′-Morpholinoacetophenone undergoes ruthenium catalyzed step-growth copolymerization with 1,3-divinyltetramethyldisiloxane to give high molecular weight copolymers.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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
MKCF7976
MKBQ3103V
10503KE
17714ES
12621JR

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Ruthenium-Catalyzed Regioselective Step-Growth Copolymerization of p-(Dialkylamino) acetophenones and. alpha.,. omega.-Dienes.
Guo H, et al.
Macromolecules, 28(13), 4714-4718 (1995)

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