NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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methyl (2S)-2-phenyl-2-[(2R)-piperidin-2-yl]acetate hydrochloride
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IUPAC Traditional name
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methyl (2S)-2-phenyl-2-[(2R)-piperidin-2-yl]acetate hydrochloride
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Synonyms
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(αR,2S)-rel-α-Phenyl-2-piperidineacetic Acid Methyl Ester Hydrochloride
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(R*,S*)-(+/-)-α-Phenyl-2-piperidineacetic Acid Methyl Ester Hydrochloride
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(+/-)-erythro-Meridil
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rac-erythro Methylphenidate Hydrochloride
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(2S,2’R)-(-)-threo-Methyl α-Phenyl-α-(2-piperidyl)acetate Hydrochloride
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(αS,2R)-α-Phenyl-2-piperidineacetic Acid Methyl Ester Hydrochloride
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(-)-erythro-Methylphenidate Hydrochloride
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D-erythro-Methylphenidate Hydrochloride
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CAS Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
Data Source
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Data ID
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Price
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TRC
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CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
H Acceptors
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2
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H Donor
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1
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LogD (pH = 5.5)
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-0.8258359
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LogD (pH = 7.4)
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0.5692904
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Log P
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2.254935
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Molar Refractivity
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66.7282 cm3
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Polarizability
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26.621723 Å3
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Polar Surface Area
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38.33 Å2
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Rotatable Bonds
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4
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Lipinski's Rule of Five
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true
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PROPERTIES
PROPERTIES
Safety Information
Product Information
Bioassay(PubChem)
DETAILS
DETAILS
TRC
Toronto Research Chemicals -
M325681
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Controlled substance. The erythro isomers have been shown to exhibit very little therapeutic effect and contribute mainly to the toxic hypertensive effects of this drug. |
Toronto Research Chemicals -
M325670
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The erythro isomers have been shown to exhibit very little therapeutic effect and contribute mainly to the toxic hypertensive effects of this drug.Controlled substance. |
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Greenblatt, E.N., et al.: J. Pharmacol. Exp. Ther., 131, 115 (1961)
- • Padmanabhan, G.R., et al.: Anal. Profiles Drug Subs., 10, 473 (1961)
- • Kuczenski, R., et al.: J. Pharmacol. Exp. Ther., 296, 876 (1961)
- • Pelham, W.E., et al.: J. Consult. Clin. Psychol.,
- • Greenblatt, E.N., et al.: J. Pharmacol. Exp. Ther., 131, 115 (1961)
- • Padmanabhan, G.R., et al.: Anal. Profiles Drug Subs., 10, 473 (1961)
- • Kuczenski, R., et al.: J. Pharmacol. Exp. Ther., 296, 876 (1961)
- • Pelham, W.E., et al.: J. Consult. Clin. Psychol.,
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PATENTS
PATENTS
PubChem Patent
Google Patent