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Benzeneacetamide, 4-(pentyloxy)-, also known as 4-(Amyloxy) acetanilide or Pentyloxy acetanilide, is an organic compound with the chemical formula C13H19NO2. It is a derivative of benzeneacetamide, featuring a pentyloxy group (C5H11O) attached to the 4-position of the benzene ring. Benzeneacetamide, 4-(pentyloxy)- is characterized by its amine and ether functional groups, which contribute to its chemical properties. It is a colorless to pale yellow liquid with a mild, aromatic odor. Benzeneacetamide, 4-(pentyloxy)-, is used in various applications, including as a chemical intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as in the production of dyes and other specialty chemicals. Its unique structure and properties make it a valuable component in the development of new compounds with specific therapeutic or industrial applications.

5100-05-0

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5100-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5100-05-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,0 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5100-05:
(6*5)+(5*1)+(4*0)+(3*0)+(2*0)+(1*5)=40
40 % 10 = 0
So 5100-05-0 is a valid CAS Registry Number.

5100-05-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-pentoxyphenyl)acetamide

1.2 Other means of identification

Product number -
Other names 4-Pentyloxy-phenyl-acetamid

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:5100-05-0 SDS

5100-05-0Upstream product

5100-05-0Downstream Products

5100-05-0Relevant 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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