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(S)-N,N-diisopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenylpropanamine L-hydrogen tartrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

873551-03-2

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873551-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 873551-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,5,5 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 873551-03:
(8*8)+(7*7)+(6*3)+(5*5)+(4*5)+(3*1)+(2*0)+(1*3)=182
182 % 10 = 2
So 873551-03-2 is a valid CAS Registry Number.

873551-03-2 Well-known Company Product Price

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  • USP

  • (1671468)  Tolterodine S-Enantiomer  United States Pharmacopeia (USP) Reference Standard

  • 873551-03-2

  • 1671468-15MG

  • 14,500.98CNY

  • Detail

873551-03-2Downstream Products

873551-03-2Relevant academic research and scientific papers

Process for the preparation of N,N-diisopropyl-3-(2-hydroxy-5-methylphenyl)- 3-phenyl propylamine and its salts starting from a novel intermediate

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Page/Page column 11, (2012/07/28)

The invention concerns an improved process for the preparation of tolterodine (N,N-diisopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenyl propylamine) and its salts, in particular for the preparation of the tartrate salt, and more in particular for the (+)-(R) enantiomer of tolterodine L-tartrate, starting from a novel intermediate, N,N-diisopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenyl-2-propenamide which can be used as pure Z or E isomer or as a mixture of Z and E isomers.

PROCESS FOR THE PREPARATION OF N,N-DIISOPROPYL-3-(2-HYDROXY-5-METHYLPHENYL)- 3-PHENYL PROPYLAMINE AND ITS SALTS STARTING FROM A NOVEL INTERMEDIATE

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Page/Page column 24, (2012/08/07)

The invention concerns an improved process for the preparation of tolterodine (N,N-diisopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenyl propyl amine) and its salts, in particular for the preparation of the tartrate salt, and more particularly for the (+)-(R) enantiomer of tolterodine L-tartrate, starting from a novel intermediate, N,N-diisopropyl-3-(2-hydroxy-5-methylphenyl)-3- phenyl-2-propenamide, which can be used as pure Z or E isomer or as a mixture of Z and E isomers. When the target is the preparation of the enantiomer (R)-(+)-(N,N- diisopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenylpropylamine) and diastereomeric crystallization of suitable compound is applied, the present invention covers also the use of racemisation of undesired (S)-(-)- (N,N-diisopropyl-3-(2-hydroxy-5-methylphenyl)-3 -phenyl propylamine) enantiomer and its recycle in the process.

A process for the purification of tolterodine

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Page/Page column 3, (2010/11/28)

Process for the purification of tolterodine comprising reacting racemic tolterodine with sulfuric acid to obtain an addition salt and racemic tolterodine acid sulfate in the crystalline form.

TOLTERODINE, COMPOSITIONS AND USES THEREOF, AND PREPARATION OF THE SAME

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Page/Page column 16, (2008/06/13)

Racemic tolterodine free base in crystalline form, tolterodine with improved purity, compositions and uses thereof, and processes of preparing the same.

An improved, scalable, and impurity-free process for tolterodine tartrate

Srinivas, Keesari,Srinivasan, Neti,Reddy, Kikkuru Srirami,Ramakrishna, Muddasani,Reddy, Chinta Raveendra,Arunagiri, Muthulingam,Kumari, Routhu Lalitha,Venkataraman, Sundaram,Mathad, Vijayavitthal T.

, p. 314 - 318 (2012/12/24)

Tolterodine tartrate is an anticholinergic muscle relaxant used to treat urinary frequency, urinary urgency, and incontinence in people with unstable bladders. An improved, cost-effective, and impurity-free process for tolterodine tartrate suitable for la

ENANTIOSELECTIVE SYNTHESIS OF ENANTIOMERICALLY ENRICHED COMPOUNDS

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Page/Page column 13, (2010/02/10)

Method of preparing an enantiomerically enriched compound of formula (II) comprising enantioselective hydrogenation of a compound of general formula (I): where W, X and Z have the meanings indicated in the description, to give a compound of general formula (II): where W, Y, T and C* have the meanings indicated in the description, in the presence of a catalyst or its suitable precursor based on Rh, Ru or Ir, having an oxidation state of 0, +1 or +2, and containing at least one enantiomerically enriched chiral ligand.

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