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4-M-TOLYL-PIPERIDIN-4-OL, also known as 4-methyl-piperidin-4-ol, is an organic compound with the chemical formula C11H17NO. It is a piperidine derivative, commonly used as an intermediate in the synthesis of various pharmaceuticals. This chemical is a colorless to pale yellow liquid, with a pleasant odor. It is also used as a building block for the manufacturing of chemicals and other organic compounds. Its applications also include its use in the production of fragrances and flavorings. 4-M-TOLYL-PIPERIDIN-4-OL has multiple industrial and pharmaceutical uses due to its stable and versatile chemical properties.

71916-57-9

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71916-57-9 Usage

Uses

Used in Pharmaceutical Industry:
4-M-TOLYL-PIPERIDIN-4-OL is used as an intermediate in the synthesis of various pharmaceuticals for its versatile chemical properties and ability to be incorporated into a wide range of drug molecules.
Used in Chemical Manufacturing:
4-M-TOLYL-PIPERIDIN-4-OL is used as a building block for the manufacturing of chemicals and other organic compounds, contributing to the development of new chemical entities and products.
Used in Fragrance and Flavoring Industry:
4-M-TOLYL-PIPERIDIN-4-OL is used as a component in the production of fragrances and flavorings, adding to the diversity of scents and tastes in various consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 71916-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,9,1 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71916-57:
(7*7)+(6*1)+(5*9)+(4*1)+(3*6)+(2*5)+(1*7)=139
139 % 10 = 9
So 71916-57-9 is a valid CAS Registry Number.

71916-57-9SDS

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-methylphenyl)piperidin-4-ol

1.2 Other means of identification

Product number -
Other names 4-M-TOLYL-PIPERIDIN-4-OL

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:71916-57-9 SDS

71916-57-9Relevant academic research and scientific papers

DIPHENYLBUTYPIPERIDINE AUTOPHAGY INDUCERS

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Page/Page column 7; 84-85, (2011/12/02)

Autophagy inducing compounds, methods of their preparation and use, and kits containg said compounds are disclosed herein.

Synthesis and SAR study of diphenylbutylpiperidines as cell autophagy inducers

Chen, Gang,Xia, Hongguang,Cai, Yu,Ma, Dawei,Yuan, Junying,Yuan, Chengye

scheme or table, p. 234 - 239 (2011/02/26)

A novel series of diphenylbutylpiperidines as autophagy inducers was described and extensive SAR studies resulted in derivatives (15d-e, 15i-j) with 10-fold greater activity than the lead compounds 1 and 2. Meanwhile, a new synthetic route to diphenylbutyl bromide (6) from bromobenzene and γ-butyrolactone was also reported here.

INDAZOLE COMPOUND AND PHARMACEUTICAL USE THEREOF

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Page/Page column 25, (2010/11/24)

The present invention can provide a cancer treatment drug containing, as an active ingredient, a substance selected from the group consisting of an indazole compound of the following formula (I), a pharmaceutically acceptable salt, a hydrate, a water adduct and a solvate:

Piperazinylacylpiperidine derivatives, their preparation and therapeutic use thereof

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Page/Page column 14, (2008/06/13)

The invention relates to substituted 1-piperazinylacylpiperidine derivatives of general formula (I) in which: n is 1 or 2; p is 1 or 2; R1 represents a halogen atom; a trifluoromethyl radical; a (C1-C4)alkyl; a (C1-C4)alkoxy; a trifluoromethoxy radical; R2 represents a hydrogen atom or a halogen atom; R3 represents a hydrogen atom; a group —OR5; a group —CH2OR5; a group —NR6R7; a group —NR8COR9; a group —NR8CONR10R11; a group —CH2NR12R13; a group —CH2NR8CONR14R15; a (C1-C4)alkoxycarbonyl; a group —CONR16R17; or else R3 constitutes a double bond between the carbon atom to which it is attached and the adjacent carbon atom of the piperidine ring; R4 represents an aromatic group selected from: the said aromatic groups being unsubstituted or being mono- or disubstituted by a substituent selected independently from a halogen atom; a (C1-C4)alkyl; a (C1-C4)alkoxy; a trifluoromethyl radical; Preparation process and therapeutic application.

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