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34333-72-7 molecular structure
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(2R)-N-(2,6-dimethylphenyl)-1-methylpiperidine-2-carboxamide hydrochloride

ChemBase ID: 172674
Molecular Formular: C15H23ClN2O
Molecular Mass: 282.80892
Monoisotopic Mass: 282.14989105
SMILES and InChIs

SMILES:
C1CCN([C@H](C1)C(=O)Nc1c(cccc1C)C)C.Cl
Canonical SMILES:
CN1CCCC[C@@H]1C(=O)Nc1c(C)cccc1C.Cl
InChI:
InChI=1S/C15H22N2O.ClH/c1-11-7-6-8-12(2)14(11)16-15(18)13-9-4-5-10-17(13)3;/h6-8,13H,4-5,9-10H2,1-3H3,(H,16,18);1H/t13-;/m1./s1
InChIKey:
RETIMRUQNCDCQB-BTQNPOSSSA-N

Cite this record

CBID:172674 http://www.chembase.cn/molecule-172674.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(2R)-N-(2,6-dimethylphenyl)-1-methylpiperidine-2-carboxamide hydrochloride
IUPAC Traditional name
mepivacaine hydrochloride hydrochloride
Synonyms
(2R)-N-(2,6-Dimethylphenyl)-1-methyl-2-piperidinecarboxamide Hydrochloride
(-)-Mepivacaine Hydrochloride
(R)-Mepivacaine Hydrochloride
D-(-)-Mepivacaine Hydrochloride
D-Mepivacaine Hydrochloride
(R)-N-(2,6-Dimethylphenyl)-1-methyl-2-piperidinecarboxamide Hydrochloride
(R)-(-)-Mepivacaine Hydrochloride
CAS Number
34333-72-7
PubChem SID
164228584
PubChem CID
53244553

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
TRC M225070 external link Add to cart
PubChem 53244553 external link
Data Source Data ID Price
TRC
M225070 external link Add to cart Please log in.
Data Source Data ID
PubChem 53244553 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 13.623901  H Acceptors
H Donor LogD (pH = 5.5) 1.4378594 
LogD (pH = 7.4) 2.9576306  Log P 3.1916199 
Molar Refractivity 76.3197 cm3 Polarizability 28.751305 Å3
Polar Surface Area 32.34 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
MSDS Link
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Certificate of Analysis
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DETAILS

DETAILS

TRC TRC
Toronto Research Chemicals - M225070 external link
An optical isomer of the local anesthetic Mepivacaine (M225060) that is slightly more active than its (+)-isomer.

REFERENCES

REFERENCES

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  • • Luduena, F.P. et al.: Arch. Int. Pharmacodyn. Ther., 200, 359 (1972)
  • • Jeske, A.H. et al.: Meth. Find. Exp. Clin. Pharmacol., 3, 33 (1972)
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PATENTS

PATENTS

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INTERNET

INTERNET

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