Cas no 533-32-4 (Butanamide,N,N-diethyl-3-methyl-)
533-32-4 structure
Product Name:Butanamide,N,N-diethyl-3-methyl-
Butanamide,N,N-diethyl-3-methyl- Chemical and Physical Properties
Names and Identifiers
-
- Butanamide,N,N-diethyl-3-methyl-
- N,N-diethyl-3-methylbutanamide
- N,N-diethylisovaleramide
- AC1L29FV
- AC1Q5IDT
- Butanamide,N-diethyl-3-methyl-
- Isovaleriansaeure-diaethylamid
- Isovaleryl diethylamide
- Isovaleryldiaethylamin
- N,N-Diaethyl-isovaleramid
- N,N-diethyl-3-methyl-butanamide
- N,N-diethyl-3-methyl-butyramide
- N,N-diethyl-isovaleramide
- Valimyl
- Valyl
- Xalyl
- Butanamide, N,N-diethyl-3-methyl-
- NSC32522
- ISOVALERYL DIETHYLAMIDE [MI]
- Q27273817
- EINECS 208-562-0
- NSC 32522
- Butyramide,N-diethyl-3-methyl-
- N,N-DIETHYL-3-METHYLBUTYRAMIDE
- NS00032720
- DTXSID50201444
- 533-32-4
- NSC-32522
- UNII-A9RAN1A34P
- SCHEMBL77705
- A9RAN1A34P
- AKOS002951434
- CHEBI:134787
- AI3-31410
-
- Inchi： 1S/C9H19NO/c1-5-10(6-2)9(11)7-8(3)4/h8H,5-7H2,1-4H3
- InChI Key： QZMQDHNCNUGQSO-UHFFFAOYSA-N
- SMILES： O=C(CC(C)C)N(CC)CC
Computed Properties
- Exact Mass: 157.14677
- Monoisotopic Mass: 157.147
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 11
- Rotatable Bond Count: 4
- Complexity: 117
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 20.3A^2
- XLogP3: 1.7
Experimental Properties
- Density: d20 0.8764
- Boiling Point: bp 210-212°; bp14 93-95°; bp5 77-78°
- Flash Point: 78.7°C
- Refractive Index: nD20 1.4422
- PSA: 20.31
- LogP: 1.90090
Butanamide,N,N-diethyl-3-methyl- Related Literature
-
Mark D. Allendorf,Alauddin Ahmed,Tom Autrey,Jeffrey Camp,Eun Seon Cho,Maciej Haranczyk,Abhi Karkamkar,Di-Jia Liu,Katie R. Meihaus,Iffat H. Nayyar,Roman Nazarov,Donald J. Siegel,Vitalie Stavila,Jeffrey J. Urban,Srimukh Prasad Veccham,Brandon C. Wood Energy Environ. Sci., 2018,11, 2784-2812
-
Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
-
Sandip Gangadhar Balwe,Yeon Tae Jeong Org. Biomol. Chem., 2018,16, 1287-1296
-
P. K. Wawrzyniak,M. T. P. Beerepoot,H. J. M. de Groot,F. Buda Phys. Chem. Chem. Phys., 2011,13, 10270-10279
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