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996-50-9 | N,N-Diethyl-1,1,1-trimethylsilanamine
CAS No: 996-50-9 Catalog No: AG003SJ6 MDL No:MFCD00009040
Product Description
Catalog Number:
AG003SJ6
Chemical Name:
N,N-Diethyl-1,1,1-trimethylsilanamine
CAS Number:
996-50-9
Molecular Formula:
C7H19NSi
Molecular Weight:
145.3180
MDL Number:
MFCD00009040
IUPAC Name:
N-ethyl-N-trimethylsilylethanamine
InChI:
InChI=1S/C7H19NSi/c1-6-8(7-2)9(3,4)5/h6-7H2,1-5H3
InChI Key:
JOOMLFKONHCLCJ-UHFFFAOYSA-N
SMILES:
CCN([Si](C)(C)C)CC
EC Number:
213-637-6
NSC Number:
377650
Properties
Complexity:
71.5
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
145.129g/mol
Formal Charge:
0
Heavy Atom Count:
9
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
145.321g/mol
Monoisotopic Mass:
145.129g/mol
Rotatable Bond Count:
3
Topological Polar Surface Area:
3.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
| Title | Journal |
|---|---|
| Aminodifluorosulfinium salts: selective fluorination reagents with enhanced thermal stability and ease of handling. | The Journal of organic chemistry 20100521 |
| Study of the chemical derivatization of zearalenone and its metabolites for gas chromatography-mass spectrometry analysis of environmental samples. | Journal of chromatography. A 20080509 |
| Nonvolatile oxidation products of glucose in Maillard model systems: formation of saccharinic and aldonic acids and their corresponding lactones. | Journal of agricultural and food chemistry 20080312 |
| Mechanism of formation of redox-active hydroxylated benzenes and pyrazine in 13C-labeled glycine/D-glucose model systems. | Journal of agricultural and food chemistry 20051214 |
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