N-Boc-1,2,3,6-tetrahydropyridine-4-boronic Acid - CAS 844501-00-4
Catalog: |
BB037198 |
Product Name: |
N-Boc-1,2,3,6-tetrahydropyridine-4-boronic Acid |
CAS: |
844501-00-4 |
Synonyms: |
[1-[(2-methylpropan-2-yl)oxy-oxomethyl]-3,6-dihydro-2H-pyridin-4-yl]boronic acid; [1-[(2-methylpropan-2-yl)oxycarbonyl]-3,6-dihydro-2H-pyridin-4-yl]boronic acid |
IUPAC Name: | [1-[(2-methylpropan-2-yl)oxycarbonyl]-3,6-dihydro-2H-pyridin-4-yl]boronic acid |
Description: | N-Boc-1,2,3,6-tetrahydropyridine-4-boronic Acid (CAS# 844501-00-4) is a useful research chemical. |
Molecular Weight: | 227.07 |
Molecular Formula: | C10H18NO4B |
Canonical SMILES: | B(C1=CCN(CC1)C(=O)OC(C)(C)C)(O)O |
InChI: | InChI=1S/C10H18BNO4/c1-10(2,3)16-9(13)12-6-4-8(5-7-12)11(14)15/h4,14-15H,5-7H2,1-3H3 |
InChI Key: | WHYUAGZAHLUISP-UHFFFAOYSA-N |
MDL: | MFCD09997795 |
LogP: | 0.50350 |
Publication Number | Title | Priority Date |
CN-111217693-A | method for preparing a, β -unsaturated carboxylic acid by reacting alkenyl boron compound catalyzed by cuprous halide with carbon dioxide | 20200219 |
US-2021300912-A1 | Aryl hydrocarbon receptor (ahr) agonists and uses thereof | 20191220 |
CN-112574189-A | EP300/CBP inhibitor | 20190927 |
WO-2021057915-A1 | Ep300/cbp inhibitor | 20190927 |
WO-2020200316-A1 | Pyrazolopyridine compound as ret inhibitor and application thereof | 20190403 |
Complexity: | 296 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 227.1328882 |
Formal Charge: | 0 |
Heavy Atom Count: | 16 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 227.1328882 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 70 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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