(S)-N-Benzyl-1-(1-naphthyl)ethylamine Hydrochloride - CAS 163831-66-1
Catalog: |
BB012043 |
Product Name: |
(S)-N-Benzyl-1-(1-naphthyl)ethylamine Hydrochloride |
CAS: |
163831-66-1 |
Synonyms: |
(1S)-1-(1-naphthalenyl)-N-(phenylmethyl)ethanamine;hydrochloride; (1S)-N-benzyl-1-naphthalen-1-ylethanamine;hydrochloride |
IUPAC Name: | (1S)-N-benzyl-1-naphthalen-1-ylethanamine;hydrochloride |
Description: | (S)-N-Benzyl-1-(1-naphthyl)ethylamine Hydrochloride (CAS# 163831-66-1) is a useful research chemical. |
Molecular Weight: | 297.82 |
Molecular Formula: | C19H20ClN |
Canonical SMILES: | CC(C1=CC=CC2=CC=CC=C21)NCC3=CC=CC=C3.Cl |
InChI: | InChI=1S/C19H19N.ClH/c1-15(20-14-16-8-3-2-4-9-16)18-13-7-11-17-10-5-6-12-19(17)18;/h2-13,15,20H,14H2,1H3;1H/t15-;/m0./s1 |
InChI Key: | KCLJDAVYFCDIDY-RSAXXLAASA-N |
Boiling Point: | 430.6 °C at 760 mmHg |
Purity: | ≥ 96 % |
MDL: | MFCD00214136 |
LogP: | 5.88350 |
Precautionary Statement: | P261 - P305 - P351 - P338 |
Publication Number | Title | Priority Date |
WO-2021210920-A1 | Method for producing ramelteon, and intermediate compound used for same | 20200416 |
CN-113473975-A | Process for preparing functionalized cyclooctenes | 20181010 |
US-2009203763-A1 | Substituted benzhydrylethers | 20080122 |
WO-2009094457-A2 | Substituted benzhydrylethers | 20080122 |
US-2008300316-A1 | Substituted phenethylamines | 20070604 |
Complexity: | 282 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 2 |
Defined Atom Stereocenter Count: | 1 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 297.1284273 |
Formal Charge: | 0 |
Heavy Atom Count: | 21 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 297.1284273 |
Rotatable Bond Count: | 4 |
Topological Polar Surface Area: | 12 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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