Ethyl 2-(1-Boc-4-piperidinyl)propanoate - CAS 141060-29-9
Catalog: |
BB009150 |
Product Name: |
Ethyl 2-(1-Boc-4-piperidinyl)propanoate |
CAS: |
141060-29-9 |
Synonyms: |
4-(1-ethoxy-1-oxopropan-2-yl)-1-piperidinecarboxylic acid tert-butyl ester; tert-butyl 4-(1-ethoxy-1-oxopropan-2-yl)piperidine-1-carboxylate |
IUPAC Name: | tert-butyl 4-(1-ethoxy-1-oxopropan-2-yl)piperidine-1-carboxylate |
Description: | Ethyl 2-(1-Boc-4-piperidinyl)propanoate (CAS# 141060-29-9 ) is a useful research chemical. |
Molecular Weight: | 285.38 |
Molecular Formula: | C15H27NO4 |
Canonical SMILES: | CCOC(=O)C(C)C1CCN(CC1)C(=O)OC(C)(C)C |
InChI: | InChI=1S/C15H27NO4/c1-6-19-13(17)11(2)12-7-9-16(10-8-12)14(18)20-15(3,4)5/h11-12H,6-10H2,1-5H3 |
InChI Key: | RNLTXXKJKMKCDZ-UHFFFAOYSA-N |
Storage: | Sealed in dry, 2-8 °C |
LogP: | 2.77060 |
Publication Number | Title | Priority Date |
US-2020299258-A1 | Quinoline and quinazoline compounds and methods of use thereof | 20190319 |
WO-2020190912-A1 | Quinoline and quinazoline compounds and methods of use thereof | 20190319 |
WO-2018068295-A1 | ARYL AND HETEROARYL ETHER DERIVATIVES AS LIVER X RECEPTOR β AGONISTS, COMPOSITIONS, AND THEIR USE | 20161014 |
US-2020247754-A1 | Aryl and heteroaryl ether derivatives as liver x receptor beta agonists, compositions, and their use | 20161014 |
AU-2010222672-A1 | Compounds for the treatment of metabolic disorders | 20090312 |
Complexity: | 340 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 285.19400834 |
Formal Charge: | 0 |
Heavy Atom Count: | 20 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 285.19400834 |
Rotatable Bond Count: | 6 |
Topological Polar Surface Area: | 55.8 |
Undefined Atom Stereocenter Count: | 1 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.6 |
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