3-(tert-Butyldimethylsilyloxy)glutaric Acid - CAS 113794-48-2
Catalog: |
BB003225 |
Product Name: |
3-(tert-Butyldimethylsilyloxy)glutaric Acid |
CAS: |
113794-48-2 |
Synonyms: |
3-[tert-butyl(dimethyl)silyl]oxypentanedioic acid; 3-[tert-butyl(dimethyl)silyl]oxypentanedioic acid |
IUPAC Name: | 3-[tert-butyl(dimethyl)silyl]oxypentanedioic acid |
Description: | 3-(tert-Butyldimethylsilyloxy)glutaric Acid (CAS# 113794-48-2 ) is a useful research chemical. |
Molecular Weight: | 262.37 |
Molecular Formula: | C11H22O5Si |
Canonical SMILES: | CC(C)(C)[Si](C)(C)OC(CC(=O)O)CC(=O)O |
InChI: | InChI=1S/C11H22O5Si/c1-11(2,3)17(4,5)16-8(6-9(12)13)7-10(14)15/h8H,6-7H2,1-5H3,(H,12,13)(H,14,15) |
InChI Key: | OHPIOMMEWYTXCL-UHFFFAOYSA-N |
LogP: | 2.32620 |
Publication Number | Title | Priority Date |
CN-110561843-A | Down fabric | 20190718 |
WO-2014195965-A2 | An improved process for the preparation of hmg-coa reductase inhibitor intermediates | 20130527 |
ES-2608787-T3 | 1H-indole-3-carboxamide derivatives and their uses as P2Y12 antagonists | 20121026 |
US-2014349350-A1 | Novel Process for the Preparation of Intermediates of HMG-CoA Reductase Inhibitors | 20111128 |
EP-2032586-A2 | A process for preparing intermediates of hmg-coa reductase inhibitors | 20070418 |
Complexity: | 277 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 262.12365033 |
Formal Charge: | 0 |
Heavy Atom Count: | 17 |
Hydrogen Bond Acceptor Count: | 5 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 262.12365033 |
Rotatable Bond Count: | 7 |
Topological Polar Surface Area: | 83.8 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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