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63843-39-0

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63843-39-0 Usage

General Description

3-(P-Tolyloxy)Piperidine is a chemical compound with the molecular formula C12H17NO. It is part of the piperidine and phenol chemical classes, which are mainly used in the pharmaceutical industry for the production of various drugs and therapeutic agents. Characterized by a benzene connected to a piperidine ring through an oxygen atom, its structural properties enhance its compatibility for chemical reactions. Its properties could potentially make it useful in the development of compounds requiring similar chemical structures. Just like any chemical compound, caution should be taken in handling 3-(P-Tolyloxy)Piperidine due to the potential risks associated with exposure or incorrect usage.

Check Digit Verification of cas no

The CAS Registry Mumber 63843-39-0 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, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63843-39:
(7*6)+(6*3)+(5*8)+(4*4)+(3*3)+(2*3)+(1*9)=140
140 % 10 = 0
So 63843-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c1-10-4-6-11(7-5-10)14-12-3-2-8-13-9-12/h4-7,12-13H,2-3,8-9H2,1H3

63843-39-0SDS

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 3-(4-methylphenoxy)piperidine

1.2 Other means of identification

Product number -
Other names 3-(P-TolYl-Oxy)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:63843-39-0 SDS

63843-39-0Relevant articles and documents

N- versus O-arylation of aminoalcohols: Orthogonal selectivity in copper-based catalysts

Shafir, Alexandr,Lichtor, Phillip A.,Buchwald, Stephen L.

, p. 3490 - 3491 (2008/01/01)

Two complementary protocols for copper-catalyzed arylation of aminoalcohols were developed. Selective N-arylation was accomplished at room temperature using 2-isobutyrylcyclohexanone (a β-diketone) as supporting ligand, while selective O-arylation require

Method of treating pain and hypertension

-

, (2008/06/13)

3-[2-(Phenyloxycycloazalkyl)ethyl]indoles possessing antihypertensive, analgesic, and tranquilizing properties and process for their preparation are described.

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