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Hydroxy Ebastine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

210686-41-2

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210686-41-2 Usage

Chemical Properties

Tan Solid

Uses

Different sources of media describe the Uses of 210686-41-2 differently. You can refer to the following data:
1. A metabolite of Ebastine
2. A metabolite of Ebastine.

Check Digit Verification of cas no

The CAS Registry Mumber 210686-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,6,8 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 210686-41:
(8*2)+(7*1)+(6*0)+(5*6)+(4*8)+(3*6)+(2*4)+(1*1)=112
112 % 10 = 2
So 210686-41-2 is a valid CAS Registry Number.
InChI:InChI=1/C32H39NO3/c1-32(2,24-34)28-17-15-25(16-18-28)30(35)14-9-21-33-22-19-29(20-23-33)36-31(26-10-5-3-6-11-26)27-12-7-4-8-13-27/h3-8,10-13,15-18,29,31,34H,9,14,19-24H2,1-2H3

210686-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-benzhydryloxypiperidin-1-yl)-1-[4-(1-hydroxy-2-methylpropan-2-yl)phenyl]butan-1-one

1.2 Other means of identification

Product number -
Other names 2-(4-(1-Oxo-4-(4-(hydroxydiphenylmethyl)-1-piperidinyl)-butyl)-phenyl)-2-methyl-propanol

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:210686-41-2 SDS

210686-41-2Upstream product

210686-41-2Downstream Products

210686-41-2Relevant academic research and scientific papers

Biooxidation of methyl group: application to the preparation of alcohol and acid metabolites of terfenadine, ebastine and analogues

El Ouarradi, Amane,Salard-Arnaud, Isabelle,Buisson, Didier

, p. 11738 - 11744 (2008)

The aim of this study was to found the best conditions to prepare metabolites of terfenadine, ebastine and analogues. For that purpose we investigated the structural substrate requirements needed for the oxidative whole cell activity and selected the most efficient conditions to obtain each compound. Our results showed that either alcohol or acid derivative arising from the oxidation of a methyl group is the main product, ratio depending on the microorganism used and on the culture conditions of cells. The oxidized metabolites were synthesized at preparative scale and isolated in 35-88% yield before characterization.

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