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4-Pentyloxybenzylamine is an organic compound with the chemical formula C12H19NO. It is a derivative of benzylamine, featuring a 4-pentyloxy group attached to the benzene ring. 4-PENTYLOXYBENZYLAMINE is characterized by its amine functional group, which consists of a nitrogen atom bonded to one or more carbon atoms. 4-Pentyloxybenzylamine is a colorless liquid with a distinct amine-like odor and is soluble in organic solvents. It is used in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products due to its versatile chemical structure. The compound is also known for its potential applications in the development of new materials and as a building block in the creation of more complex organic molecules.

5085-43-8

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5085-43-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5085-43-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,8 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5085-43:
(6*5)+(5*0)+(4*8)+(3*5)+(2*4)+(1*3)=88
88 % 10 = 8
So 5085-43-8 is a valid CAS Registry Number.

5085-43-8SDS

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 4-PENTYLOXYBENZYLAMINE

1.2 Other means of identification

Product number -
Other names 4-N-PENTYLOXYBENZYLAMINE

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 -
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More Details:5085-43-8 SDS

5085-43-8Relevant academic research and scientific papers

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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