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Hydroxyamfetamine

PubChem CID: 3651

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Compound Synonyms 4-(2-Aminopropyl)phenol, hydroxyamphetamine, 103-86-6, Hydroxyamfetamine, 4-Hydroxyamphetamine, Norveritol, Pulsoton, Paredrine, p-HYDROXYAMPHETAMINE, Norpholedrine, Oxamphetamine, Oxamphetaminium, Oksamfetamin, Oxamfetamin, Paredrinex, Nov-Pholedrin, Phenol, 4-(2-aminopropyl)-, Paradrine, Pedrolon, p-(2-Aminopropyl)phenol, Phenol, p-(2-aminopropyl)-, DL-p-Hydroxyamphetamine, Phenol,4-(2-aminopropyl)-, 1-p-Hydroxyphenyl-2-propylamine, dl-4-hydroxyamphetamine, 2-Amino-1-(p-hydroxyphenyl)propane, .alpha.-Methyltyramine, NSC 170995, Hydroxyamfetamine [INN], Hidroxianfetamina, alpha-Methyltyramine, p-Hydroxy-alpha-methylphenethylamine, Racemic p-hydroxyamphetamine, 4-Hydroxy-alpha-methylphenethylamine, EINECS 203-152-8, FQR280JW2N, Hydroxyamfetamine [INN:BAN], 4-Hydroxy-.alpha.-methylphenethylamine, NSC-170995, BRN 2413849, DL-p-(2-Aminopropyl)phenol, HYDROXYAMPHETAMINE [MI], 1518-86-1, HYDROXYAMPHETAMINE [VANDF], HYDROXYAMFETAMINE [WHO-DD], 3-13-00-01709 (Beilstein Handbook Reference), p-Hydroxy-.alpha.-methylphenethylamine, (+/-)-P-(2-AMINOPROPYL)PHENOL, Hydroxyamphetamide, 4-(2-aminopropyl)phenol, hydrobromide, UNII-FQR280JW2N, idrossiamfetamina, hydroxyamfetaminum, Predrolon (Salt/Mix), Spectrum_001243, OH-A, Spectrum3_001037, Spectrum4_001174, Spectrum5_001674, (RS)-4-hydroxyamphetamine, Hydroxyamphetamine,(+/-), WLN: Z3R DQ, CHEMBL1546, 4-(2-amino-propyl)-phenol, BSPBio_002853, KBioGR_001807, KBioSS_001723, (+/-)-4-Hydroxyamphetamine, SCHEMBL125440, DTXSID3023134, BDBM81459, KBio2_001723, KBio2_004291, KBio2_006859, KBio3_002073, CHEBI:103855, AAA10386, HY-B1098, NSC_3651, 1-(4-Hydroxyphenyl)propane-2-amine, NSC170995, PDSP1_001107, PDSP2_001091, AKOS000155358, AKOS017269170, CS-4687, DB09352, benzene, 1-(2-amino)propyl-4-hydroxy-, NCGC00178433-01, NCGC00178433-02, BS-13447, CAS_103-86-6, DB-229149, NS00006145, Phenol, p-(2-aminopropyl)-, (.+/-.)-, EN300-53926, Phenol, 4-(2-aminopropyl)-, (.+/-.)-, AB01563354_01, Q5955531, BRD-A80871782-004-01-0, BRD-A80871782-004-06-9, Z57102382, 203-152-8
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 46.3
Hydrogen Bond Donor Count 2.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCCCC1
Np Classifier Class Phenylalanine-derived alkaloids
Deep Smiles CCCcccccc6))O))))))N
Heavy Atom Count 11.0
Classyfire Class Benzene and substituted derivatives
Scaffold Graph Node Level C1CCCCC1
Classyfire Subclass Phenethylamines
Isotope Atom Count 0.0
Molecular Complexity 108.0
Database Name hmdb_chem_all;imppat_phytochem;pubchem
Defined Atom Stereocenter Count 0.0
Iupac Name 4-(2-aminopropyl)phenol
Class Benzene and substituted derivatives
Veber Rule True
Classyfire Superclass Benzenoids
Xlogp 1.4
Superclass Benzenoids
Subclass Phenethylamines
Gsk 4 400 Rule True
Molecular Formula C9H13NO
Scaffold Graph Node Bond Level c1ccccc1
Inchi Key GIKNHHRFLCDOEU-UHFFFAOYSA-N
Silicos It Class Soluble
Rotatable Bond Count 2.0
Synonyms HYDROXYAMFETAMINE, Hydrobromide, hydroxyamphetamine, Hydroxyamphetamin, Hydroxyamphetamine hydrobromide, Norpholedrin, Oxyamphetamine, p-Hydroxyamphetamine, Para hydroxyamphetamine, Hydroxyphenylisopropylamine, Paredrine, p Hydroxyamphetamine, Para-hydroxyamphetamine, Methyltyramine, Hydroxyamphetamine, phenol, 4-(2-aminopropyl)-
Esol Class Very soluble
Functional Groups CN, cO
Compound Name Hydroxyamfetamine
Kingdom Organic compounds
Exact Mass 151.1
Formal Charge 0.0
Monoisotopic Mass 151.1
Hydrogen Bond Acceptor Count 2.0
Molecular Weight 151.21
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 1.0
Total Bond Stereocenter Count 0.0
Molecular Framework Aromatic homomonocyclic compounds
Lipinski Rule Of 5 True
Inchi InChI=1S/C9H13NO/c1-7(10)6-8-2-4-9(11)5-3-8/h2-5,7,11H,6,10H2,1H3
Smiles CC(CC1=CC=C(C=C1)O)N
Np Classifier Biosynthetic Pathway Alkaloids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Taxonomy Direct Parent Amphetamines and derivatives
Np Classifier Superclass Pseudoalkaloids

  • 1. Outgoing r'ship FOUND_IN to/from Glycyrrhiza Glabra (Plant) Rel Props:Reference:https://doi.org/10.1080/0972060x.2011.10643935