4-Acetylmorpholine - CAS 1696-20-4
Catalog: |
BB012564 |
Product Name: |
4-Acetylmorpholine |
CAS: |
1696-20-4 |
Synonyms: |
1-morpholin-4-ylethanone |
IUPAC Name: | 1-morpholin-4-ylethanone |
Description: | 4-Acetylmorpholine (CAS# 1696-20-4) is a useful research chemical. |
Molecular Weight: | 129.16 |
Molecular Formula: | C6H11NO2 |
Canonical SMILES: | CC(=O)N1CCOCC1 |
InChI: | InChI=1S/C6H11NO2/c1-6(8)7-2-4-9-5-3-7/h2-5H2,1H3 |
InChI Key: | KYWXRBNOYGGPIZ-UHFFFAOYSA-N |
Boiling Point: | 245.5 °C |
Melting Point: | 41892 °C |
Purity: | 95 % |
Density: | 1.116 g/cm3 |
Appearance: | Clear colourless to very slightly yellow liquid |
Storage: | Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. |
MDL: | MFCD00006171 |
LogP: | -0.19700 |
GHS Hazard Statement: | H315 (45.5%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P201, P202, P261, P264, P272, P280, P281, P302+P352, P305+P351+P338, P308+P313, P321, P332+P313, P333+P313, P337+P313, P362, P363, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-112812241-A | Controlled-activity photocuring 3D printing resin and preparation method and application thereof | 20210122 |
CN-112870983-A | Method for desorbing CO from organic solvent2The preparation method of the polyimide film | 20210114 |
CN-112903834-A | Detection method for morpholine residue in bulk drug and application thereof | 20201123 |
WO-2021100881-A2 | Method for producing fullerene derivative-containing resin composition, fullerene derivative-containing resin composition obtained from same, resin paint, resin coating, and enamel wire | 20200330 |
JP-2021155699-A | Polishing composition, its manufacturing method, polishing method and semiconductor substrate manufacturing method | 20200325 |
PMID | Publication Date | Title | Journal |
21837155 | 20110701 | (Z)-3-(3,4-Dimeth-oxy-phen-yl)-3-(4-fluoro-phen-yl)-1-morpholino-prop-2-en-1-one | Acta crystallographica. Section E, Structure reports online |
16388636 | 20060106 | Synthesis and aqueous chemistry of alpha-acetoxy-N-nitrosomorpholine: reactive intermediates and products | The Journal of organic chemistry |
Complexity: | 108 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 129.078978594 |
Formal Charge: | 0 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 129.078978594 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 29.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | -0.7 |
-
Catalog: BB026817
N,N'-Dicyclohexyl-4-morpholinecarboxamidine
Detail
-
Catalog: BB003037
(2S,3R)-N-Boc-6-oxo-2,3-diphenylmorpholine
Detail
-
Catalog: BB002238
N-Ethyl-2-morpholin-4-ylethanamine
Detail
-
Catalog: BB018496
2-(2,6-Dimethylmorpholin-4-yl)ethanamine
Detail
-
Catalog: BB022035
Morpholine-2,2,3,3,5,5,6,6-D8
Detail
-
Catalog: BB009127
4-(4-Bromo-2,6-difluorophenyl)morpholine
Detail
-
Catalog: BB022405
(S)-3-Methylmorpholine
Detail
-
Catalog: BB018272
2-Phenylmorpholine Hydrochloride
Detail
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Morpholines/Thiomorpholines
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS