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1-(2-Piperidinophenyl)-ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78648-37-0

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78648-37-0 Usage

Type of compound

Organic compound

Structural features

Contains a piperidine ring
Contains a phenyl ring
Has an ethanol group attached to the piperidine ring

Applications

Used in organic synthesis
Used in pharmaceutical research as a building block for the synthesis of various drug molecules

Pharmacological activities

Studied for potential analgesic effects
Studied for potential anti-inflammatory effects

Toxicity

Moderate toxicity; should be handled with care in laboratory settings

Check Digit Verification of cas no

The CAS Registry Mumber 78648-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,4 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78648-37:
(7*7)+(6*8)+(5*6)+(4*4)+(3*8)+(2*3)+(1*7)=180
180 % 10 = 0
So 78648-37-0 is a valid CAS Registry Number.

78648-37-0Relevant academic research and scientific papers

SULFONANILIDE AND BENZYLSULFONYL DERIVATIVES, AND COMPOSITIONS AND METHODS THEREOF

-

, (2022/04/16)

The invention provides novel sulfonanilide and benzylsulfonyl derivatives, and compositions and methods of preparation and use thereof, that are useful in treating various diseases and disorders related to TRPML activities such as lysosome storage diseases, muscular dystrophy, age-related common neurodegenerative diseases, oxidative stress or reactive oxygen species (ROS) related diseases, and ageing.

Synthesis, structure and N-N bonding character of 1,1-disubstituted indazolium hexafluorophosphate

Ning, Yingtang,Kawahata, Masatoshi,Yamaguchi, Kentaro,Otani, Yuko,Ohwada, Tomohiko

, p. 1881 - 1884 (2018/02/23)

1,1-Disubstituted indazolium hexafluorophosphates were synthesized via intramolecular electrophilic amination reactions under mild conditions. The crystal structures were determined and are consistent with the presence of a stable N-N bond, which can be cleaved by hydrogenation. Both experimental and computational studies suggest a covalent bonding character of the N-N bond, with diminished aromaticity of the newly formed pyrazolium ring due to the quaternary ammonium atom (N1), in contrast to the aromatic character of the parent indazole.

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