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17879-45-7 | Acetamide, 2,2-bis(trimethylsilyl)-
CAS No: 17879-45-7 Catalog No: AG0026AX MDL No:
Product Description
Catalog Number:
AG0026AX
Chemical Name:
Acetamide, 2,2-bis(trimethylsilyl)-
CAS Number:
17879-45-7
Molecular Formula:
C8H21NOSi2
Molecular Weight:
203.4294
IUPAC Name:
2,2-bis(trimethylsilyl)acetamide
InChI:
InChI=1S/C8H21NOSi2/c1-11(2,3)8(7(9)10)12(4,5)6/h8H,1-6H3,(H2,9,10)
InChI Key:
NDVMCQUOSYOQMZ-UHFFFAOYSA-N
SMILES:
NC(=O)C([Si](C)(C)C)[Si](C)(C)C
Properties
Complexity:
165
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
203.116g/mol
Formal Charge:
0
Heavy Atom Count:
12
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
203.432g/mol
Monoisotopic Mass:
203.116g/mol
Rotatable Bond Count:
3
Topological Polar Surface Area:
43.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
| Title | Journal |
|---|---|
| First total synthesis of a naturally occurring iodinated 5'-deoxyxylofuranosyl marine nucleoside. | Marine drugs 20120401 |
| 3,3'-Dinitro-bis-phenol A. | Acta crystallographica. Section E, Structure reports online 20111001 |
| In situ carboxyl activation using a silatropic switch: a new approach to amide and peptide constructions. | Journal of the American Chemical Society 20110914 |
| Conformationally constrained histidines in the design of peptidomimetics: strategies for the χ-space control. | International journal of molecular sciences 20110101 |
| Identification of ascorbic acid and its degradation products in black powder substitutes. | Journal of forensic sciences 20040501 |
| Microwave-accelerated derivatization processes for the determination of phenolic acids by gas chromatography-mass spectrometry. | Talanta 20010706 |
| Preparation of silyl enol ethers using (bistrimethylsilyl)acetamide in ionic liquids. | Organic letters 20010405 |
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