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19395-41-6

  • Product NameRitalinic acid
  • Molecular FormulaC13H17NO2
  • Molecular Weight219.283
  • Purity99%
  • AppearanceOff-white solid
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  • CasNo: 19395-41-6
  • Molecular Formula: C13H17NO2
  • Appearance: Off-white solid
  • Purity: 99%

Fast Delivery Ritalinic Acid 19395-41-6

19395-41-6 Name

Name

Ritalinic acid

Synonym

alpha-Phenylpiperidine-2-acetic acid;a-Phenyl-2-piperidineacetic Acid;Ritainic Acid;α-Phenyl-2-piperidineacetic acid;α-phenylpiperidine-2-acetic acid;Ritalinic acid/alpha-Phenylpiperidine-2-acetic acid;2-Piperidineacetic acid, alpha-phenyl-;alpha-Phenyl-2-piperidineacetic acid

 

Ritalinic Acid 19395-41-6 In Bulk Supply

19395-41-6 Chemical & Physical Properties

Melting point 

236-238ºC

Boiling point

367.7±17.0 °C at 760 mmHg

Density

1.1±0.1 g/cm3

Molecular Formula

C13H17NO2

Molecular Weight

219.280

Flash Point

176.2±20.9 °C

PSA

49.33000

LogP

2.08

Exact Mass

219.125931

Vapour Pressure

0.0±0.9 mmHg at 25°C

Index of Refraction

1.554

 

19395-41-6 Uses

A major metabolite of Methylphenidate.

 

 

 

Relevant articles

 

 

Microtubing-Reactor-Assisted Aliphatic C?H Functionalization with HCl as a Hydrogen-Atom-Transfer Catalyst Precursor in Conjunction with an Organic Photoredox Catalyst

 

Deng, Hong-Ping,Zhou, Quan,Wu, Jie

, p. 12661 - 12665 (2018/09/20)

Chlorine radical, which is classically generated by the homolysis of Cl2 under UV irradiation, can abstract a hydrogen atom from an unactivated C(sp3)?H bond. We herein demonstrate the use of HCl as an effective hydrogen-atom-transfer catalyst precursor activated by an organic acridinium photoredox catalyst under visible-light irradiation for C?H alkylation and allylation.


Synthesis and pharmacology of potential cocaine antagonists. 2. Structure-activity relationship studies of aromatic ring-substituted methylphenidate analogs

 

Deutsch, Howard M.,Shi, Qing,Gruszecka-Kowalik, Ewa,Schwer, Margaret M.

, p. 1201 - 1209 (2007/10/03)

As part of a program, to develop medications which can block the binding of cocaine to the dopamine transporter, yet spare dopamine uptake, a series of aromatic ring-substituted methylphenidate derivatives was synthesized and tested for inhibitory potency in [3H]WIN 35,428 binding and [3H]dopamine uptake assays using rat striatal tissue.

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