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Benzeneacetic acid, a-hydroxy-a-phenyl-, 4-piperidinyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25811-48-7

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25811-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25811-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,1 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25811-48:
(7*2)+(6*5)+(5*8)+(4*1)+(3*1)+(2*4)+(1*8)=107
107 % 10 = 7
So 25811-48-7 is a valid CAS Registry Number.

25811-48-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-benziloyloxypiperidine

1.2 Other means of identification

Product number -
Other names hydroxy-diphenyl-acetic acid piperidin-4-yl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25811-48-7 SDS

25811-48-7Relevant academic research and scientific papers

Glycolic ester derivative and its use

-

Paragraph 0066; 0067; 0068; 0069; 0070, (2017/06/29)

The invention relates to hydroxyacetic acid ester derivatives and use thereof and particularly relates to compounds shown in the formula I, or pharmaceutically acceptable salts, esters, solvates and prodrugs of the compounds, wherein R1 and R2 are respectively selected from phenyl, cyclohexyl, cyclopentyl and thienyl and are optionally substituted by 1-3 groups of hydroxy, halogen, trifluoromethyl, trifluoromethoxy, amino, carboxy, cyano, (C1-C4)alkyl, (C1-C4)alkoxy, (C1-C4)alkenyl, (C1- C4)alkynyl, N-(C1-C4)alkylamino. The invention further relates to a method for preparing the compounds, pharmaceutical compositions containing the compounds and pharmaceutical use of the compounds. The compound provided by the invention can be used for treating respiratory system diseases including but not limited to asthma, chronic obstructive pulmonary disease and the like.

Biomimetic investigations of propiverinhydrochloride and 1-methyl-4-piperidyl benzilate

Froehlich,Pietzyk,Smolinka,Goeber

, p. 745 - 747 (2007/10/03)

The reaction of propiverinhydrochloride (1) and 1-methyl-4-piperidyl benzilate (2) with the biomimetic system manganese(III)-5,10,15,20-tetrakis(pentafluorophenyl)-β-tetrasulfonat oporphyrin chloride (MnTPFPS4PCl)/imidazole/hydrogen peroxide in aqueous solution at pH 7-8 affords unchanged 1 and 2 and numerous metabolites, which are products of fission of the ester bond, of O-dealkylation, decarboxylation, N-demethylation, and oxidation of the tertiary amine function. In contrast to the nonaqueous system with the catalyst manganese(III)-5,10,15,20-tetrakis(pentafluorophenyl)porphyrin chloride (MnTPFPPCl) aromatic hydroxylation is not observed. This result shows conformity with the studies of metabolism in men.

Biomimetic oxidation of propiverinhydrochloride and 1-methyl-4-piperidyl benzilate

Frohlich,Pietzyk,Gober

, p. 736 - 740 (2007/10/03)

The reaction of propiverinhydrochloride (1) and 1-methyl-4-piperidyl benzilate (2) with the biomimetic system manganese(III)-5,10,15,20-tetrakis(pentafluorophenyl)porphyrin chloride (MnTPFPPCl)/pyridine/hydrogen peroxide affords unchanged 1 and 2 and 15 potential metabolites, which were isolated and identified. These compounds are products of cleavage of the ester bond, of O-dealkylation, aromatic oxidation, respectively of decarboxylation, demethylation, and N-oxidation. Products were identified by TLC, UV, and MS in comparison with authentic samples. Thereby we found a nearly conformity with rat metabolism.

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