(S)-3-[(tert-Butyldimethylsilyl)oxy]-2-methyl-1-propanol - CAS 105859-45-8
Catalog: |
BB001732 |
Product Name: |
(S)-3-[(tert-Butyldimethylsilyl)oxy]-2-methyl-1-propanol |
CAS: |
105859-45-8 |
Synonyms: |
(2S)-3-[tert-butyl(dimethyl)silyl]oxy-2-methyl-1-propanol; (2S)-3-[tert-butyl(dimethyl)silyl]oxy-2-methylpropan-1-ol |
IUPAC Name: | (2S)-3-[tert-butyl(dimethyl)silyl]oxy-2-methylpropan-1-ol |
Description: | (S)-3-[(tert-Butyldimethylsilyl)oxy]-2-methyl-1-propanol (CAS# 105859-45-8) is a compound useful in organic synthesis. |
Molecular Weight: | 204.38 |
Molecular Formula: | C10H24O2Si |
Canonical SMILES: | CC(CO)CO[Si](C)(C)C(C)(C)C |
InChI: | InChI=1S/C10H24O2Si/c1-9(7-11)8-12-13(5,6)10(2,3)4/h9,11H,7-8H2,1-6H3/t9-/m0/s1 |
InChI Key: | OAWLYVJZJYEJSM-VIFPVBQESA-N |
Boiling Point: | 232.222 °C at 760 mmHg |
Density: | 0.875 g/cm3 |
LogP: | 2.63660 |
Publication Number | Title | Priority Date |
US-2015246938-A1 | Novel olefin derivative | 20110909 |
JP-2003252870-A | 14-membered macrolide compound | 20020226 |
EP-1301472-A2 | Oxygenated esters of 4-iodo phenylamino benzhydroxamic acids | 20000719 |
WO-0206213-A2 | Oxygenated esters of 4-iodo phenylamino benzhydroxamic acids | 20000719 |
EP-0389244-A1 | Process for synthesis of FK-506 C10-C18 intermediates | 19890323 |
Complexity: | 150 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 204.154556538 |
Formal Charge: | 0 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 204.154556538 |
Rotatable Bond Count: | 5 |
Topological Polar Surface Area: | 29.5 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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