Methyl (1-Benzyl-4-methyl-3-piperidyl)carbamate Hydrochloride - CAS 1206824-67-0
Catalog: |
BB004927 |
Product Name: |
Methyl (1-Benzyl-4-methyl-3-piperidyl)carbamate Hydrochloride |
CAS: |
1206824-67-0 |
Synonyms: |
N-[4-methyl-1-(phenylmethyl)-3-piperidinyl]carbamic acid methyl ester;hydrochloride; methyl N-(1-benzyl-4-methylpiperidin-3-yl)carbamate;hydrochloride |
IUPAC Name: | methyl N-(1-benzyl-4-methylpiperidin-3-yl)carbamate;hydrochloride |
Description: | Methyl (1-Benzyl-4-methyl-3-piperidyl)carbamate Hydrochloride (CAS# 1206824-67-0 ) is a useful research chemical. |
Molecular Weight: | 298.81 |
Molecular Formula: | C15H23ClN2O2 |
Canonical SMILES: | CC1CCN(CC1NC(=O)OC)CC2=CC=CC=C2.Cl |
InChI: | InChI=1S/C15H22N2O2.ClH/c1-12-8-9-17(10-13-6-4-3-5-7-13)11-14(12)16-15(18)19-2;/h3-7,12,14H,8-11H2,1-2H3,(H,16,18);1H |
InChI Key: | HIBZBVJEHDKCNZ-UHFFFAOYSA-N |
LogP: | 3.38380 |
Publication Number | Title | Priority Date |
WO-2020204647-A1 | Processes for preparing (3r,4r)-1-benzyl-n,4-dimethylpiperidin-3-amine or a salt thereof and processes for preparing tofacitinib using the same | 20190405 |
CN-104860872-A | Bis-(3R,4R)-1-benzyl-N,4-dimethyl piperidin-3-amine L-di-p-toluyl tartrate synthesis method | 20150327 |
AU-2010292487-A1 | Heterocyclic compounds as janus kinase inhibitors | 20090827 |
CA-2770712-A1 | Heterocyclic compounds as janus kinase inhibitors | 20090827 |
JP-2013503191-A | Heterocyclic compounds as Janus kinase inhibitors | 20090827 |
Complexity: | 290 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 2 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 298.1448057 |
Formal Charge: | 0 |
Heavy Atom Count: | 20 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 298.1448057 |
Rotatable Bond Count: | 4 |
Topological Polar Surface Area: | 41.6 |
Undefined Atom Stereocenter Count: | 2 |
Undefined Bond Stereocenter Count: | 0 |
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