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63843-46-9

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63843-46-9 Usage

Uses

4-(3-Methylphenoxy)piperidine is used as pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 63843-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,4 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63843-46:
(7*6)+(6*3)+(5*8)+(4*4)+(3*3)+(2*4)+(1*6)=139
139 % 10 = 9
So 63843-46-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c1-10-3-2-4-12(9-10)14-11-5-7-13-8-6-11/h2-4,9,11,13H,5-8H2,1H3

63843-46-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H50950)  4-(3-Methylphenoxy)piperidine, 97%   

  • 63843-46-9

  • 250mg

  • 428.0CNY

  • Detail
  • Alfa Aesar

  • (H50950)  4-(3-Methylphenoxy)piperidine, 97%   

  • 63843-46-9

  • 1g

  • 1714.0CNY

  • Detail

63843-46-9SDS

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 4-(3-METHYLPHENOXY)PIPERIDINE

1.2 Other means of identification

Product number -
Other names 4-m-tolyloxy-piperidine

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:63843-46-9 SDS

63843-46-9Upstream product

63843-46-9Downstream Products

63843-46-9Relevant articles and documents

Piperidylalkylindoles. 1. Hypotensive activity of 3-[2-(phenoxypiperidyl)ethyl]indoles

Helsley,Strupczewski,Woodward

, p. 309 - 312 (2007/10/05)

A series of 3-[2-(phenoxypiperidyl)ethyl]indoles was synthesized and evaluated for hypotensive activity in the spontaneous hypertensive rat. Maximum hypotensive activity appeared when the phenoxy substituent was para substituted and occupied the 4 position of the piperidine ring.

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