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121522-27-8 | 3-Butyn-2-ol, 4-(trimethylsilyl)-, (2S)-
CAS No: 121522-27-8 Catalog No: AG00158J MDL No:
Product Description
Catalog Number:
AG00158J
Chemical Name:
3-Butyn-2-ol, 4-(trimethylsilyl)-, (2S)-
CAS Number:
121522-27-8
Molecular Formula:
C7H14OSi
Molecular Weight:
142.2710
IUPAC Name:
4-trimethylsilylbut-3-yn-2-ol
InChI:
InChI=1S/C7H14OSi/c1-7(8)5-6-9(2,3)4/h7-8H,1-4H3
InChI Key:
HJJSDJHRTMFJLP-UHFFFAOYSA-N
SMILES:
C[C@@H](C#C[Si](C)(C)C)O
Properties
Complexity:
143
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
142.081g/mol
Formal Charge:
0
Heavy Atom Count:
9
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
142.273g/mol
Monoisotopic Mass:
142.081g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
20.2A^2
Undefined Atom Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Literature
| Title | Journal |
|---|---|
| Efficient asymmetric reduction of 4-(trimethylsilyl)-3-butyn-2-one by Candida parapsilosis cells in an ionic liquid-containing system. | PloS one 20120101 |
| Optimization of culture conditions to produce high yields of active Acetobacter sp. CCTCC M209061 cells for anti-Prelog reduction of prochiral ketones. | BMC biotechnology 20110101 |
| Using a water-immiscible ionic liquid to improve asymmetric reduction of 4-(trimethylsilyl)-3-butyn-2-one catalyzed by immobilized Candida parapsilosis CCTCC M203011 cells. | BMC biotechnology 20090101 |
| Lipase-mediated resolution of 4-TMS-3-butyn-2-ol and use of the mesylate derivatives as a precursor to a highly stereoselective chiral allenylindium reagent. | Organic letters 20011018 |
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