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2-[4-(2-methoxyphenyl)piperazin-1-yl]-1-pyridin-3-ylethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58012-94-5

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58012-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58012-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,1 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58012-94:
(7*5)+(6*8)+(5*0)+(4*1)+(3*2)+(2*9)+(1*4)=115
115 % 10 = 5
So 58012-94-5 is a valid CAS Registry Number.

58012-94-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(2-methoxyphenyl)piperazin-1-yl]-1-pyridin-3-ylethanol

1.2 Other means of identification

Product number -
Other names -

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:58012-94-5 SDS

58012-94-5Upstream product

58012-94-5Relevant academic research and scientific papers

Process for the preparation of 1-pyridyl-alkyl-4-aryl piperazines which are useful as antihypertensive compounds, their separation into the respective optical antipodes, and the stereoisomeric compounds so obtained

-

, (2008/06/13)

A process for the preparation of 1-pyridyl-alkyl-4-aryl piperazines, in the racemic form, of the formula STR1 in which: the pyridine ring is alpha-, beta-, or gamma-substituted; R=H; Cn H2n+1, n being in the range from 1 to 4; R'=H, halogen, CH3, OCH3, in which process: (a) pyridine aldehyde is reacted between -5° C. and 0° C. with (CH3)2 S=CH2 ; (b) the oxirane so obtained is treated with an arylpiperazine; (c) the hydroxyl derivative obtained in (b), after salification with alkaline hydrides or hydrates in a solvent medium is treated with alkylating agents, and the separation of the compounds so obtained into the respective optical antipodes.

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