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65423-11-2

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65423-11-2 Usage

General Description

2-(4-butoxyphenyl)ethanamine is a chemical compound with the molecular formula C12H19NO. It is an amine derivative and a member of the phenethylamine family. The compound consists of a phenyl ring with a butoxy group attached to it along with an ethanamine group, which is a secondary amine. 2-(4-butoxyphenyl)ethanamine is used in the field of medicinal chemistry and drug development, particularly in the synthesis of various pharmaceuticals and psychoactive substances. Additionally, it may have potential applications in neuroscience and pharmacology research due to its effects on the central nervous system. However, it is important to handle and use this chemical with caution and in accordance with proper safety protocols and regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 65423-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,2 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65423-11:
(7*6)+(6*5)+(5*4)+(4*2)+(3*3)+(2*1)+(1*1)=112
112 % 10 = 2
So 65423-11-2 is a valid CAS Registry Number.

65423-11-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Butoxyphenyl)ethanamine

1.2 Other means of identification

Product number -
Other names 4-butoxyphenethylamine

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:65423-11-2 SDS

65423-11-2Relevant articles and documents

Design of Inhibitors from the Three-Dimensional Structure of Alcohol Dehydrogenase. Chemical Synthesis and Enzymatic Properties

Freudenreich, Charles,Samama, Jean-Pierre,Biellmann, Jean-Francois

, p. 3344 - 3353 (2007/10/02)

Inhibitors of liver alcohol dehydrogenase were designed from the three-dimensional structure of the enzyme.The ligand to the catalytic zinc ion is an amide group or, better, a formamide group.With the latter function, a hydrogen bond between the NH group and the hydroxyl group of Ser-48 may be formed.The hydrophobic substrate binding site brings structural restraints. α-ω bifunctional molecules show good inhibitory properties possibly due to the interactions with polar residues at the entrance of the substrate binding site.

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